Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145400.1 | 312 | Intron | NP_001138872.1 | ||
NM_139174.3 | 312 | Missense Mutation | CGC,CTC | R168L | NP_631913.3 |
XM_005255814.1 | 312 | Intron | XP_005255871.1 | ||
XM_011522919.1 | 312 | Missense Mutation | CGC,CTC | R168L | XP_011521221.1 |
XM_011522920.1 | 312 | Missense Mutation | CGC,CTC | R38L | XP_011521222.1 |