Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001289097.1 | 1791 | Intron | NP_001276026.1 | ||
NM_032876.5 | 1791 | Missense Mutation | CCC,CTC | P472L | NP_116265.1 |
NM_198086.2 | 1791 | Missense Mutation | CCC,CTC | P55L | NP_932352.1 |