Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001160047.1 | 2806 | Missense Mutation | CCG,CTG | P786L | NP_001153519.1 |
NM_020784.2 | 2806 | Missense Mutation | CCG,CTG | P791L | NP_065835.2 |
XM_017021505.1 | 2806 | Intron | XP_016876994.1 |