Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000238.3 | 3167 | Missense Mutation | CAG,GAG | Q1119E | NP_000229.1 |
NM_001204798.1 | 3167 | Intron | NP_001191727.1 | ||
NM_172056.2 | 3167 | Intron | NP_742053.1 | ||
NM_172057.2 | 3167 | Missense Mutation | CAG,GAG | Q779E | NP_742054.1 |
XM_011516185.2 | 3167 | Missense Mutation | CAG,GAG | Q1019E | XP_011514487.1 |
XM_011516186.2 | 3167 | Intron | XP_011514488.1 | ||
XM_017012195.1 | 3167 | Missense Mutation | CAG,GAG | Q1069E | XP_016867684.1 |
XM_017012196.1 | 3167 | Missense Mutation | CAG,GAG | Q1060E | XP_016867685.1 |