Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001001694.2 | 2113 | Missense Mutation | CCG,CTG | P239L | NP_001001694.2 |
XM_011530689.2 | 2113 | Missense Mutation | CCG,CTG | P311L | XP_011528991.1 |
XM_017028798.1 | 2113 | Missense Mutation | CCG,CTG | P311L | XP_016884287.1 |