Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_181684.2 | 465 | Missense Mutation | ATC,GTC | I142V | NP_859012.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001272037.1 | 465 | Intron | NP_001258966.1 | ||
NM_144991.2 | 465 | Intron | NP_659428.2 |