Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001102612.2 | 726 | Missense Mutation | GCG,GTG | A142V | NP_001096082.2 |
NM_001167902.1 | 726 | Intron | NP_001161374.1 | ||
XM_011521254.1 | 726 | Missense Mutation | GCG,GTG | A233V | XP_011519556.1 |
XM_017021933.1 | 726 | Missense Mutation | GCG,GTG | A88V | XP_016877422.1 |