Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005112.4 | 2199 | Missense Mutation | CGG,TGG | R435W | NP_005103.2 |
NM_017491.3 | 2199 | Missense Mutation | CGG,TGG | R575W | NP_059830.1 |
XM_017008880.1 | 2199 | Missense Mutation | CGG,TGG | R628W | XP_016864369.1 |