Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001014980.2 | 900 | Silent Mutation | GTC,GTT | V258V | NP_001014980.1 |
XM_011541435.2 | 900 | Missense Mutation | TCT,TTT | S263F | XP_011539737.1 |
XM_011541436.2 | 900 | Missense Mutation | TCT,TTT | S257F | XP_011539738.1 |
XM_011541437.1 | 900 | Missense Mutation | TCT,TTT | S191F | XP_011539739.1 |