Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001122955.3 | 1680 | Missense Mutation | AAG,GAG | K390E | NP_001116427.1 |
NM_001130702.2 | 1680 | Silent Mutation | CCA,CCG | P278P | NP_001124174.2 |
NM_032667.6 | 1680 | Missense Mutation | AAG,GAG | K326E | NP_116056.3 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_203422.3 | 1680 | Intron | NP_981967.1 |