Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001318043.1 | 208 | Missense Mutation | CGG,TGG | R10W | NP_001304972.1 |
NM_080820.5 | 208 | Missense Mutation | CGG,TGG | R10W | NP_543010.3 |
XM_005260872.4 | 208 | Intron | XP_005260929.1 |