Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003215.2 | 2942 | Missense Mutation | CGG,TGG | R549W | NP_003206.2 |
XM_011513737.2 | 2942 | Missense Mutation | CGG,TGG | R513W | XP_011512039.1 |
XM_011513741.1 | 2942 | Intron | XP_011512043.1 | ||
XM_017008569.1 | 2942 | Missense Mutation | CGG,TGG | R433W | XP_016864058.1 |