Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000039.2 | 637 | Missense Mutation | CCC,CGC | P189R | NP_000030.1 |
NM_001318017.1 | 637 | Missense Mutation | CCC,CGC | P189R | NP_001304946.1 |
NM_001318018.1 | 637 | Missense Mutation | CCC,CGC | P189R | NP_001304947.1 |
NM_001318021.1 | 637 | Missense Mutation | CCC,CGC | P80R | NP_001304950.1 |