Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001014980.2 | 982 | Missense Mutation | ATC,GTC | I286V | NP_001014980.1 |
XM_011541435.2 | 982 | Silent Mutation | CCA,CCG | P290P | XP_011539737.1 |
XM_011541436.2 | 982 | Silent Mutation | CCA,CCG | P284P | XP_011539738.1 |
XM_011541437.1 | 982 | Silent Mutation | CCA,CCG | P218P | XP_011539739.1 |