Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006767.3 | 992 | Intron | NP_006758.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001008695.1 | 992 | Missense Mutation | CAG,CGG | Q263R | NP_001008695.1 |
NM_030573.2 | 992 | Missense Mutation | CAG,CGG | Q263R | NP_085050.2 |