Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006277.2 | 5162 | Missense Mutation | CAG,CCG | Q1662P | NP_006268.2 |
NM_019595.3 | 5162 | Missense Mutation | CAG,CCG | Q1635P | NP_062541.3 |
NM_147152.2 | 5162 | Intron | NP_671494.2 |