Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_007361.3 | 4156 | Missense Mutation | CGG,TGG | R1308W | NP_031387.3 |
XM_005267405.4 | 4156 | Missense Mutation | CGG,TGG | R1335W | XP_005267462.1 |
XM_005267406.4 | 4156 | Missense Mutation | CGG,TGG | R1287W | XP_005267463.1 |
XM_005267407.4 | 4156 | Missense Mutation | CGG,TGG | R1260W | XP_005267464.1 |