Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006454.2 | 571 | Missense Mutation | GCG,GTG | A180V | NP_006445.1 |
XM_011513388.2 | 571 | Missense Mutation | GCG,GTG | A234V | XP_011511690.1 |
XM_017007655.1 | 571 | Intron | XP_016863144.1 | ||
XM_017007656.1 | 571 | Intron | XP_016863145.1 |