| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001283014.1 | 266 | Missense Mutation | ACC,GCC | T22A | NP_001269943.1 |
| NM_001283015.1 | 266 | Missense Mutation | ACC,GCC | T22A | NP_001269944.1 |
| NM_001283016.1 | 266 | UTR 5 | NP_001269945.1 | ||
| NM_001283017.1 | 266 | UTR 5 | NP_001269946.1 | ||
| NM_001283019.1 | 266 | UTR 5 | NP_001269948.1 | ||
| NM_015901.5 | 266 | Missense Mutation | ACC,GCC | T22A | NP_056985.3 |
| XM_017016033.1 | 266 | Missense Mutation | ACC,GCC | T22A | XP_016871522.1 |