Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000041.3 | 162 | Intron | NP_000032.1 | ||
NM_001302688.1 | 162 | Missense Mutation | AAC,AAG | N14K | NP_001289617.1 |
NM_001302689.1 | 162 | Intron | NP_001289618.1 | ||
NM_001302690.1 | 162 | Intron | NP_001289619.1 | ||
NM_001302691.1 | 162 | Intron | NP_001289620.1 |