Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000308.3 | 1382 | Missense Mutation | CAG,CGG | Q67R | NP_000299.2 |
NM_001127695.2 | 1382 | Missense Mutation | CAG,CGG | Q49R | NP_001121167.1 |
NM_001167594.2 | 1382 | Missense Mutation | CAG,CGG | Q67R | NP_001161066.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001278535.1 | 1382 | Intron | NP_001265464.1 | ||
NM_080749.3 | 1382 | Intron | NP_542787.1 |