Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001320635.1 | 438 | Missense Mutation | GCG,GTG | A23V | NP_001307564.1 |
NM_001320636.1 | 438 | Intron | NP_001307565.1 | ||
NM_020980.4 | 438 | Missense Mutation | GCG,GTG | A23V | NP_066190.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
XM_011522293.2 | 438 | Intron | XP_011520595.1 |