Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_024667.2 | 831 | Missense Mutation | CCG,CTG | P243L | NP_078943.1 |
XM_005253622.3 | 831 | Missense Mutation | CCG,CTG | P215L | XP_005253679.1 |
XM_006719602.3 | 831 | Missense Mutation | CCG,CTG | P215L | XP_006719665.1 |
XM_011538743.2 | 831 | Missense Mutation | CCG,CTG | P302L | XP_011537045.1 |
XM_011538745.2 | 831 | Missense Mutation | CCG,CTG | P225L | XP_011537047.1 |
XM_017019970.1 | 831 | Intron | XP_016875459.1 | ||
XM_017019971.1 | 831 | Intron | XP_016875460.1 | ||
XM_017019972.1 | 831 | Intron | XP_016875461.1 |