| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001194946.1 | 805 | Missense Mutation | ACC,GCC | T168A | NP_001181875.1 |
| NM_001194947.1 | 805 | Missense Mutation | ACC,GCC | T168A | NP_001181876.1 |
| NM_001291157.1 | 805 | Missense Mutation | ACC,GCC | T121A | NP_001278086.1 |
| NM_004953.4 | 805 | Intron | NP_004944.3 | ||
| NM_182917.4 | 805 | Missense Mutation | ACC,GCC | T161A | NP_886553.3 |
| NM_198241.2 | 805 | Missense Mutation | ACC,GCC | T161A | NP_937884.1 |
| NM_198242.2 | 805 | UTR 5 | NP_937885.1 | ||
| NM_198244.2 | 805 | Missense Mutation | ACC,GCC | T74A | NP_937887.1 |