Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001304829.1 | 2135 | Missense Mutation | GCG,GTG | A478V | NP_001291758.1 |
NM_194292.2 | 2135 | Missense Mutation | GCG,GTG | A645V | NP_919268.1 |
XM_017000486.1 | 2135 | Missense Mutation | GCG,GTG | A618V | XP_016855975.1 |