Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001271609.1 | 701 | Missense Mutation | CCG,CTG | P167L | NP_001258538.1 |
NM_001271610.1 | 701 | Missense Mutation | CCG,CTG | P167L | NP_001258539.1 |
NM_001271611.1 | 701 | Missense Mutation | CCG,CTG | P118L | NP_001258540.1 |
NM_003765.2 | 701 | Missense Mutation | CCG,CTG | P167L | NP_003756.1 |
XM_011528397.2 | 701 | Intron | XP_011526699.1 |