Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_145294.4 | 850 | Silent Mutation | CGG,TGG | R266W | NP_660337.3 |
XM_017023023.1 | 850 | Missense Mutation | CGG,TGG | R266W | XP_016878512.1 |
XM_017023024.1 | 850 | Intron | XP_016878513.1 |