Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000845.2 | 3569 | Missense Mutation | AGT,ATT | S902I | NP_000836.2 |
NM_001127323.1 | 3569 | UTR 3 | NP_001120795.1 | ||
XM_006715938.3 | 3569 | Missense Mutation | AGT,ATT | S902I | XP_006716001.1 |
XM_011516091.1 | 3569 | Missense Mutation | AGT,ATT | S902I | XP_011514393.1 |
XM_011516092.2 | 3569 | UTR 3 | XP_011514394.1 | ||
XM_011516094.1 | 3569 | UTR 3 | XP_011514396.1 | ||
XM_011516095.2 | 3569 | UTR 3 | XP_011514397.1 | ||
XM_011516101.2 | 3569 | UTR 3 | XP_011514403.1 | ||
XM_011516102.2 | 3569 | UTR 3 | XP_011514404.1 | ||
XM_011516103.2 | 3569 | UTR 3 | XP_011514405.1 | ||
XM_011516108.2 | 3569 | UTR 3 | XP_011514410.1 | ||
XM_017012074.1 | 3569 | Missense Mutation | AGT,ATT | S902I | XP_016867563.1 |
XM_017012075.1 | 3569 | Missense Mutation | AGT,ATT | S697I | XP_016867564.1 |
XM_017012076.1 | 3569 | Missense Mutation | AGT,ATT | S697I | XP_016867565.1 |
XM_017012077.1 | 3569 | Missense Mutation | AGT,ATT | S697I | XP_016867566.1 |
XM_017012078.1 | 3569 | Missense Mutation | AGT,ATT | S697I | XP_016867567.1 |
XM_017012079.1 | 3569 | Missense Mutation | AGT,ATT | S697I | XP_016867568.1 |
XM_017012080.1 | 3569 | UTR 3 | XP_016867569.1 |