Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_144715.3 | 2126 | Silent Mutation | GAC,GAT | D790D | NP_653316.3 |
XM_005264889.1 | 2126 | Missense Mutation | ACG,ATG | T783M | XP_005264946.1 |
XM_011533382.1 | 2126 | Silent Mutation | GAC,GAT | D769D | XP_011531684.1 |
XM_011533383.2 | 2126 | Silent Mutation | GAC,GAT | D412D | XP_011531685.2 |
XM_011533385.2 | 2126 | Silent Mutation | GAC,GAT | D579D | XP_011531687.1 |
XM_017005741.1 | 2126 | Silent Mutation | GAC,GAT | D660D | XP_016861230.1 |
XM_017005742.1 | 2126 | Intron | XP_016861231.1 | ||
XM_017005743.1 | 2126 | Silent Mutation | GAC,GAT | D412D | XP_016861232.1 |
XM_017005744.1 | 2126 | Silent Mutation | GAC,GAT | D412D | XP_016861233.1 |
XM_017005745.1 | 2126 | Missense Mutation | ACG,ATG | T405M | XP_016861234.1 |