Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003098.2 | 1390 | Missense Mutation | CCG,CTG | P386L | NP_003089.1 |
XM_005260517.1 | 1390 | Missense Mutation | CCG,CTG | P386L | XP_005260574.1 |
XM_011529007.1 | 1390 | Missense Mutation | CCG,CTG | P386L | XP_011527309.1 |
XM_011529008.1 | 1390 | Missense Mutation | CCG,CTG | P386L | XP_011527310.1 |