Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001304829.1 | 2122 | Missense Mutation | ACG,GCG | T474A | NP_001291758.1 |
NM_194292.2 | 2122 | Missense Mutation | ACG,GCG | T641A | NP_919268.1 |
XM_017000486.1 | 2122 | Missense Mutation | ACG,GCG | T614A | XP_016855975.1 |