Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001170796.1 | 600 | Missense Mutation | CCC,GCC | P193A | NP_001164267.1 |
NM_001170797.1 | 600 | Missense Mutation | CCC,GCC | P200A | NP_001164268.1 |
NM_024699.2 | 600 | Missense Mutation | CCC,GCC | P200A | NP_078975.2 |