Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145348.1 | 262 | Missense Mutation | GCG,GTG | A62V | NP_001138820.1 |
NM_024773.2 | 262 | Missense Mutation | GCG,GTG | A24V | NP_079049.2 |
XM_017023676.1 | 262 | Missense Mutation | GCG,GTG | A24V | XP_016879165.1 |
XM_017023677.1 | 262 | UTR 5 | XP_016879166.1 | ||
XM_017023678.1 | 262 | UTR 5 | XP_016879167.1 | ||
XM_017023679.1 | 262 | UTR 5 | XP_016879168.1 | ||
XM_017023680.1 | 262 | UTR 5 | XP_016879169.1 |