Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_016602.2 | 415 | Missense Mutation | CTC,TTC | L89F | NP_057686.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003632.2 | 415 | Intron | NP_003623.1 | ||
XM_005257748.4 | 415 | Intron | XP_005257805.1 | ||
XM_017025238.1 | 415 | UTR 5 | XP_016880727.1 |