Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145132.1 | 298 | Missense Mutation | GCG,GTG | A79V | NP_001138604.1 |
XM_011534416.1 | 298 | Missense Mutation | GCG,GTG | A79V | XP_011532718.1 |
XM_017008909.1 | 298 | Intron | XP_016864398.1 |