Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001004693.1 | 442 | Intron | NP_001004693.1 | ||
XM_017000273.1 | 442 | Intron | XP_016855762.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001001964.1 | 442 | Missense Mutation | AGG,GGG | R148G | NP_001001964.1 |