Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001010977.2 | 669 | Missense Mutation | AGG,GGG | R216G | NP_001010977.1 |
XM_017020407.1 | 669 | Missense Mutation | AGG,GGG | R216G | XP_016875896.1 |
XM_017020408.1 | 669 | Missense Mutation | AGG,GGG | R216G | XP_016875897.1 |