Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_144578.3 | 1070 | Missense Mutation | GCT,GTT | A21V | NP_653179.1 |
XM_011537362.2 | 1070 | Missense Mutation | GCT,GTT | A34V | XP_011535664.2 |
XM_017021789.1 | 1070 | Missense Mutation | GCT,GTT | A21V | XP_016877278.1 |