Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001287223.1 | 3892 | Missense Mutation | GAT,GGT | D1695G | NP_001274152.1 |
NM_014139.2 | 3892 | Missense Mutation | GAT,GGT | D1695G | NP_054858.2 |
XM_011533321.2 | 3892 | Missense Mutation | GAT,GGT | D1474G | XP_011531623.1 |
XM_017005647.1 | 3892 | Missense Mutation | GAT,GGT | D1820G | XP_016861136.1 |
XM_017005648.1 | 3892 | Missense Mutation | GAT,GGT | D1629G | XP_016861137.1 |
XM_017005649.1 | 3892 | Missense Mutation | GAT,GGT | D1695G | XP_016861138.1 |
XM_017005650.1 | 3892 | Missense Mutation | GAT,GGT | D1695G | XP_016861139.1 |
XM_017005651.1 | 3892 | Missense Mutation | GAT,GGT | D1604G | XP_016861140.1 |
XM_017005652.1 | 3892 | Intron | XP_016861141.1 | ||
XM_017005653.1 | 3892 | Missense Mutation | GAT,GGT | D1163G | XP_016861142.1 |