Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001040059.1 | 313 | Intron | NP_001035148.1 | ||
NM_001251.2 | 313 | Missense Mutation | ACG,ATG | T41M | NP_001242.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001204510.1 | 313 | Intron | NP_001191439.1 | ||
NM_001416.3 | 313 | Intron | NP_001407.1 |