Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001409.3 | 4427 | Missense Mutation | GCG,GTG | A1522V | NP_001400.3 |
XM_006710406.3 | 4427 | Missense Mutation | GCG,GTG | A1417V | XP_006710469.1 |
XM_011540885.1 | 4427 | Missense Mutation | GCG,GTG | A1584V | XP_011539187.1 |
XM_011540886.1 | 4427 | Missense Mutation | GCG,GTG | A1541V | XP_011539188.1 |
XM_011540887.2 | 4427 | Missense Mutation | GCG,GTG | A1376V | XP_011539189.1 |
XM_011540888.2 | 4427 | Intron | XP_011539190.1 | ||
XM_017000533.1 | 4427 | Missense Mutation | GCG,GTG | A1540V | XP_016856022.1 |