Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001080456.2 | 1609 | Missense Mutation | CGT,TGT | R477C | NP_001073925.2 |
XM_005258864.3 | 1609 | Missense Mutation | CGT,TGT | R530C | XP_005258921.2 |
XM_006723189.3 | 1609 | Missense Mutation | CGT,TGT | R477C | XP_006723252.1 |