Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001042616.2 | 687 | Missense Mutation | CCT,CTT | P48L | NP_001036081.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_032906.4 | 687 | UTR 3 | NP_116295.1 |