Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001308122.1 | 182 | Missense Mutation | CCG,CTG | P114L | NP_001295051.1 |
NM_003060.3 | 182 | Missense Mutation | CCG,CTG | P114L | NP_003051.1 |
XM_011543590.2 | 182 | UTR 5 | XP_011541892.1 | ||
XM_017009778.1 | 182 | UTR 5 | XP_016865267.1 |