E Homo sapiens | Beckwith-Wiedemann syndrome chromosomal region 1 c [SLC22A18AS]
Protein ID | Sequence length | Exons | Domain Architectures | Number exons | Cross reference | |
---|---|---|---|---|---|---|
HUMAN03972 | 150 | 1 | ![]() | |||
HUMAN03973 | 150 | 1 | ![]() | |||
HUMAN03971 reference isoform | 253 | 2 | ![]() |
MGELPGSEGM WENCPLGWVK KKASGTLAPL DFLLQRKRLW LWASEPVRPQ PQGIHRFREA 60 RRQFCRMRGS RLTGGRKGFG SSGLRFGRGG FSEEVMPQPV LKAMRCAEGA WWFSPDGPAG 120 SAASIWPAEG AEGLPGQLGR DRLEVVYSVP DNVPGQNGSR RPLVCKITGK CLSVCSEENA 180 KAGGCSAFPL LLSQLGARMT GREHAHKGPE LTTPDSGLPR PPNPALAGFR ALAQHSPPLG 240 TSTPSAVLLS AAT 253
ATGGGGGAAC TTCCTGGTTC TGAGGGAATG TGGGAAAATT GCCCTTTAGG CTGGGTGAAG 60 AAGAAAGCAA GTGGAACCCT GGCACCCCTG GACTTCCTCC TCCAGAGGAA GCGGCTTTGG 120 TTGTGGGCCA GCGAGCCTGT GCGTCCCCAG CCCCAGGGCA TTCACCGCTT CAGAGAAGCA 180 AGGCGACAGT TCTGCCGGAT GAGAGGATCC AGGCTGACTG GAGGAAGGAA GGGCTTTGGC 240 TCATCTGGGC TCAGGTTTGG GAGAGGTGGC TTCTCAGAGG AGGTGATGCC TCAGCCAGTC 300 TTAAAGGCAA TGCGGTGTGC AGAGGGTGCT TGGTGGTTCT CTCCTGATGG CCCCGCAGGG 360 TCTGCAGCCT CCATCTGGCC AGCAGAGGGC GCAGAAGGAC TGCCTGGGCA GCTCGGACGT 420 GACCGCCTGG AAGTGGTGTA CAGCGTTCCT GACAACGTTC CCGGCCAAAA CGGGTCCCGC 480 CGCCCACTTG TGTGCAAGAT AACTGGAAAA TGTCTTTCTG TGTGCTCCGA GGAGAATGCA 540 AAGGCTGGTG GATGTAGTGC CTTTCCTCTA CTGCTCTCTC AGCTGGGGGC AAGAATGACA 600 GGACGTGAAC ATGCACACAA GGGCCCGGAA CTCACGACCC CCGACAGCGG TCTCCCCCGC 660 CCCCCCAACC CCGCGCTTGC AGGATTTAGG GCACTAGCAC AGCACAGTCC ACCCCTTGGG 720 ACTAGCACCC CCTCCGCAGT TCTGCTCTCT GCAGCAACAT AG 762