Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001302809.1 | 439 | Missense Mutation | CCG,CTG | P26L | NP_001289738.1 |
NM_152460.2 | 439 | Missense Mutation | CCG,CTG | P26L | NP_689673.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001115152.1 | 439 | Intron | NP_001108624.1 |