Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001303253.1 | 1413 | Intron | NP_001290182.1 | ||
NM_005891.2 | 1413 | Intron | NP_005882.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001008897.1 | 1413 | Missense Mutation | CAT,CGT | H238R | NP_001008897.1 |
NM_030752.2 | 1413 | Missense Mutation | CAT,CGT | H393R | NP_110379.2 |