Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152353.2 | 1353 | Missense Mutation | GCC,GTC | A98V | NP_689566.1 |
XM_011526425.2 | 1353 | Missense Mutation | GCC,GTC | A98V | XP_011524727.1 |
XM_011526428.2 | 1353 | Missense Mutation | GCC,GTC | A98V | XP_011524730.1 |
XM_017026244.1 | 1353 | Silent Mutation | CGC,CGT | R225R | XP_016881733.1 |
XM_017026245.1 | 1353 | Silent Mutation | CGC,CGT | R225R | XP_016881734.1 |
XM_017026246.1 | 1353 | Missense Mutation | GCC,GTC | A98V | XP_016881735.1 |
XM_017026247.1 | 1353 | Silent Mutation | CGC,CGT | R225R | XP_016881736.1 |