Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000281.3 | 662 | Missense Mutation | CAG,CGG | Q88R | NP_000272.1 |
NM_001289797.1 | 662 | Missense Mutation | CAG,CGG | Q39R | NP_001276726.1 |
NM_001323004.1 | 662 | Intron | NP_001309933.1 |