Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000110.3 | 3268 | Missense Mutation | GAT,GTT | D974V | NP_000101.2 |
NM_001160301.1 | 3268 | Intron | NP_001153773.1 | ||
XM_005270562.3 | 3268 | Missense Mutation | GAT,GTT | D902V | XP_005270619.2 |
XM_006710397.3 | 3268 | Intron | XP_006710460.1 | ||
XM_017000507.1 | 3268 | Missense Mutation | GAT,GTT | D937V | XP_016855996.1 |
XM_017000508.1 | 3268 | Missense Mutation | GAT,GTT | D809V | XP_016855997.1 |
XM_017000509.1 | 3268 | Missense Mutation | GAT,GTT | D809V | XP_016855998.1 |
XM_017000510.1 | 3268 | Missense Mutation | GAT,GTT | D809V | XP_016855999.1 |