| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001136037.2 | 1167 | Missense Mutation | GAG,GTG | E319V | NP_001129509.2 |
| NM_001161403.1 | 1167 | Missense Mutation | GAG,GTG | E297V | NP_001154875.1 |
| NM_001161404.1 | 1167 | Missense Mutation | GAG,GTG | E292V | NP_001154876.1 |
| NM_001256542.1 | 1167 | Missense Mutation | GAG,GTG | E145V | NP_001243471.1 |
| NM_017980.4 | 1167 | Missense Mutation | GAG,GTG | E321V | NP_060450.2 |
| XM_005263710.2 | 1167 | Missense Mutation | GAG,GTG | E228V | XP_005263767.1 |
| XM_006712627.3 | 1167 | Missense Mutation | GAG,GTG | E181V | XP_006712690.1 |
| XM_006712628.3 | 1167 | Intron | XP_006712691.1 | ||
| XM_011511453.1 | 1167 | Missense Mutation | GAG,GTG | E280V | XP_011509755.1 |
| XM_017004469.1 | 1167 | Missense Mutation | GAG,GTG | E194V | XP_016859958.1 |