Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001200029.1 | 1289 | Missense Mutation | CAG,CGG | Q369R | NP_001186958.1 |
NM_001200030.1 | 1289 | Missense Mutation | CAG,CGG | Q339R | NP_001186959.1 |
NM_001200031.1 | 1289 | Missense Mutation | CAG,CGG | Q120R | NP_001186960.1 |
NM_001200032.1 | 1289 | Missense Mutation | CAG,CGG | Q90R | NP_001186961.1 |
NM_003549.3 | 1289 | Missense Mutation | CAG,CGG | Q369R | NP_003540.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006764.4 | 1289 | Intron | NP_006755.4 |