Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001304385.1 | 296 | Missense Mutation | CCG,CTG | P70L | NP_001291314.1 |
NM_153215.2 | 296 | Missense Mutation | CCG,CTG | P71L | NP_694947.1 |
XM_006712979.3 | 296 | Missense Mutation | CCG,CTG | P80L | XP_006713042.1 |
XM_006712980.3 | 296 | Missense Mutation | CCG,CTG | P79L | XP_006713043.1 |
XM_011533370.2 | 296 | Missense Mutation | CCG,CTG | P47L | XP_011531672.1 |