Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001193272.1 | 1712 | Intron | NP_001180201.1 | ||
NM_001193273.1 | 1712 | Missense Mutation | GCG,GTG | A395V | NP_001180202.1 |
NM_005057.3 | 1712 | Missense Mutation | GCG,GTG | A522V | NP_005048.2 |
XM_011509833.2 | 1712 | Missense Mutation | GCG,GTG | A522V | XP_011508135.1 |