Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001304522.1 | 1496 | Missense Mutation | TCC,TTC | S330F | NP_001291451.1 |
NM_001308259.1 | 1496 | Missense Mutation | TCC,TTC | S394F | NP_001295188.1 |
NM_003382.4 | 1496 | Missense Mutation | TCC,TTC | S410F | NP_003373.2 |
XM_005249561.3 | 1496 | Missense Mutation | TCC,TTC | S435F | XP_005249618.1 |
XM_006716107.2 | 1496 | Intron | XP_006716170.1 | ||
XM_006716108.3 | 1496 | Intron | XP_006716171.1 | ||
XM_011516550.2 | 1496 | Intron | XP_011514852.1 | ||
XM_017012580.1 | 1496 | Missense Mutation | TCC,TTC | S272F | XP_016868069.1 |