Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_017966.4 | 775 | Missense Mutation | CCG,CTG | P225L | NP_060436.4 |
XM_005274077.3 | 775 | Missense Mutation | CCG,CTG | P225L | XP_005274134.1 |
XM_017017955.1 | 775 | Missense Mutation | CCG,CTG | P112L | XP_016873444.1 |