Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_015506.2 | 405 | Missense Mutation | CCG,CTG | P116L | NP_056321.2 |
XM_005270724.4 | 405 | Missense Mutation | CCG,CTG | P51L | XP_005270781.1 |
XM_011541204.2 | 405 | Missense Mutation | CCG,CTG | P59L | XP_011539506.1 |