Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001301035.1 | 1167 | Missense Mutation | CCG,CGG | P306R | NP_001287964.1 |
NM_001308402.1 | 1167 | Missense Mutation | CCG,CGG | P306R | NP_001295331.1 |
NM_001312656.1 | 1167 | Missense Mutation | CCG,CGG | P306R | NP_001299585.1 |
NM_006494.3 | 1167 | Missense Mutation | CCG,CGG | P381R | NP_006485.2 |
XM_017026468.1 | 1167 | Missense Mutation | CCG,CGG | P306R | XP_016881957.1 |
XM_017026469.1 | 1167 | Missense Mutation | CCG,CGG | P306R | XP_016881958.1 |