Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001009606.3 | 822 | Missense Mutation | CCG,CTG | P199L | NP_001009606.3 |
XM_011522608.2 | 822 | Missense Mutation | CCG,CTG | P74L | XP_011520910.1 |
XM_011522609.2 | 822 | Missense Mutation | CCG,CTG | P59L | XP_011520911.1 |