Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001130448.2 | 600 | Missense Mutation | CAG,CGG | Q22R | NP_001123920.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_018163.2 | 600 | Intron | NP_060633.1 | ||
XM_017022401.1 | 600 | Intron | XP_016877890.1 | ||
XM_017022402.1 | 600 | Intron | XP_016877891.1 |