Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001122955.3 | 1657 | Missense Mutation | TCA,TTA | S382L | NP_001116427.1 |
NM_001130702.2 | 1657 | Nonsense Mutation | CAG,TAG | Q271* | NP_001124174.2 |
NM_032667.6 | 1657 | Missense Mutation | TCA,TTA | S318L | NP_116056.3 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_203422.3 | 1657 | Intron | NP_981967.1 |