Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001277081.1 | 1244 | Missense Mutation | GCG,GTG | A138V | NP_001264010.1 |
NM_001277082.1 | 1244 | Missense Mutation | GCG,GTG | A138V | NP_001264011.1 |
NM_017509.3 | 1244 | Missense Mutation | GCG,GTG | A139V | NP_059979.2 |
XM_006723265.3 | 1244 | Missense Mutation | GCG,GTG | A139V | XP_006723328.1 |
XM_011527085.2 | 1244 | Missense Mutation | GCG,GTG | A138V | XP_011525387.1 |
XM_011527087.2 | 1244 | Intron | XP_011525389.1 | ||
XM_011527088.2 | 1244 | Missense Mutation | GCG,GTG | A139V | XP_011525390.1 |
XM_011527089.2 | 1244 | Missense Mutation | GCG,GTG | A138V | XP_011525391.1 |
XM_017026943.1 | 1244 | Intron | XP_016882432.1 |