Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001286242.1 | 5989 | Missense Mutation | CGG,TGG | R2023W | NP_001273171.1 |
NM_001520.3 | 5989 | Missense Mutation | CGG,TGG | R2048W | NP_001511.2 |
XM_017023188.1 | 5989 | Missense Mutation | CGG,TGG | R1985W | XP_016878677.1 |