Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145641.1 | 107 | Missense Mutation | CCT,CGT | P29R | NP_001139113.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_182498.3 | 107 | Intron | NP_872304.2 |