Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001286474.1 | 1642 | Missense Mutation | GAT,GCT | D477A | NP_001273403.1 |
NM_001286475.1 | 1642 | Missense Mutation | GAT,GCT | D463A | NP_001273404.1 |
NM_006781.4 | 1642 | Missense Mutation | GAT,GCT | D479A | NP_006772.3 |
XM_017010182.1 | 1642 | Missense Mutation | XP_016865671.1 | ||
XM_017010183.1 | 1642 | Intron | XP_016865672.1 | ||
XM_017010184.1 | 1642 | Intron | XP_016865673.1 | ||
XM_017010185.1 | 1642 | Missense Mutation | XP_016865674.1 |