Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_178171.4 | 411 | Missense Mutation | ACG,ATG | T98M | NP_835465.2 |
XM_006721832.2 | 411 | Missense Mutation | ACG,ATG | T98M | XP_006721895.1 |
XM_011524651.2 | 411 | Intron | XP_011522953.1 | ||
XM_017024502.1 | 411 | Missense Mutation | ACG,ATG | T98M | XP_016879991.1 |
XM_017024503.1 | 411 | Missense Mutation | ACG,ATG | T98M | XP_016879992.1 |
XM_017024504.1 | 411 | Missense Mutation | ACG,ATG | T98M | XP_016879993.1 |