Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001199103.1 | 648 | Missense Mutation | CCT,CTT | P490L | NP_001186032.1 |
NM_001199104.1 | 648 | UTR 3 | NP_001186033.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_020905.3 | 648 | Missense Mutation | CCT,CTT | P176L | NP_065956.1 |