Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001005567.2 | 516 | Intron | NP_001005567.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001004756.2 | 516 | Missense Mutation | CCT,CTT | P165L | NP_001004756.2 |