Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006187.3 | 212 | Missense Mutation | CGG,TGG | R65W | NP_006178.2 |
XM_005253889.3 | 212 | Missense Mutation | CGG,TGG | R65W | XP_005253946.1 |
XM_017019363.1 | 212 | Missense Mutation | CGG,TGG | R65W | XP_016874852.1 |