Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001114331.2 | 2337 | Missense Mutation | CGG,TGG | R743W | NP_001107803.1 |
NM_001287.5 | 2337 | Missense Mutation | CGG,TGG | R767W | NP_001278.1 |
XM_011522354.1 | 2337 | Missense Mutation | CGG,TGG | R709W | XP_011520656.1 |