Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001080.3 | 38 | Missense Mutation | GGC,TGC | G4C | NP_001071.1 |
NM_170740.1 | 38 | Missense Mutation | GGC,TGC | G4C | NP_733936.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001503.3 | 38 | Intron | NP_001494.2 | ||
XM_011514509.2 | 38 | Missense Mutation | CAG,CCG | Q2P | XP_011512811.1 |
XM_017010753.1 | 38 | Missense Mutation | CAG,CCG | Q2P | XP_016866242.1 |
XM_017010754.1 | 38 | Intron | XP_016866243.1 |