Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006761.4 | 956 | Intron | NP_006752.1 | ||
XM_005256784.3 | 956 | Missense Mutation | CGG,TGG | R231W | XP_005256841.1 |
XM_017025005.1 | 956 | Missense Mutation | CGG,TGG | R209W | XP_016880494.1 |