Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001039130.1 | 592 | Missense Mutation | CCT,CGT | P159R | NP_001034219.1 |
NM_001039131.1 | 592 | Missense Mutation | CCT,CGT | P159R | NP_001034220.1 |
NM_001141.2 | 592 | Missense Mutation | CCT,CGT | P159R | NP_001132.2 |