Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_173687.3 | 732 | Missense Mutation | CCG,CTG | P39L | NP_775958.1 |
XM_017013344.1 | 732 | Missense Mutation | CCG,CTG | P34L | XP_016868833.1 |
XM_017013345.1 | 732 | Missense Mutation | CCG,CTG | P34L | XP_016868834.1 |
XM_017013346.1 | 732 | Missense Mutation | CCG,CTG | P34L | XP_016868835.1 |