Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001447.2 | 13208 | Missense Mutation | GCG,GGG | A4285G | NP_001438.1 |
XM_006714761.3 | 13208 | Missense Mutation | GCG,GGG | A4285G | XP_006714824.1 |
XM_011537600.2 | 13208 | Missense Mutation | GCG,GGG | A4285G | XP_011535902.1 |
XM_011537603.2 | 13208 | Missense Mutation | GCG,GGG | A4285G | XP_011535905.1 |
XM_017009224.1 | 13208 | Missense Mutation | GCG,GGG | A4285G | XP_016864713.1 |
XM_017009225.1 | 13208 | Missense Mutation | GCG,GGG | A4285G | XP_016864714.1 |
XM_017009226.1 | 13208 | Intron | XP_016864715.1 | ||
XM_017009227.1 | 13208 | Intron | XP_016864716.1 |