Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001014980.2 | 799 | Missense Mutation | CGG,TGG | R225W | NP_001014980.1 |
XM_011541435.2 | 799 | Silent Mutation | TGC,TGT | C229C | XP_011539737.1 |
XM_011541436.2 | 799 | Silent Mutation | TGC,TGT | C223C | XP_011539738.1 |
XM_011541437.1 | 799 | Silent Mutation | TGC,TGT | C157C | XP_011539739.1 |