Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004769.3 | 746 | Missense Mutation | CCG,CTG | P51L | NP_004760.1 |
NM_020321.3 | 746 | Missense Mutation | CCG,CTG | P51L | NP_064717.1 |
NM_020322.3 | 746 | Missense Mutation | CCG,CTG | P51L | NP_064718.1 |