Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282190.1 | 1693 | Missense Mutation | GAT,GCT | D348A | NP_001269119.1 |
NM_001282191.1 | 1693 | Intron | NP_001269120.1 | ||
NM_016478.4 | 1693 | Missense Mutation | GAT,GCT | D369A | NP_057562.3 |
XM_005250403.2 | 1693 | Missense Mutation | GAT,GCT | D245A | XP_005250460.1 |
XM_011516288.2 | 1693 | Missense Mutation | GAT,GCT | D302A | XP_011514590.1 |
XM_011516289.2 | 1693 | Missense Mutation | GAT,GCT | D279A | XP_011514591.1 |
XM_011516290.2 | 1693 | Missense Mutation | GAT,GCT | D201A | XP_011514592.1 |
XM_017012287.1 | 1693 | Missense Mutation | GAT,GCT | D326A | XP_016867776.1 |
XM_017012288.1 | 1693 | Missense Mutation | GAT,GCT | D201A | XP_016867777.1 |