Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006137.6 | 426 | Missense Mutation | CCG,CTG | P106L | NP_006128.1 |
XM_011523608.1 | 426 | Missense Mutation | CCG,CTG | P6L | XP_011521910.1 |
XM_017025316.1 | 426 | Missense Mutation | CCG,CTG | P6L | XP_016880805.1 |