| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001317997.1 | 867 | Missense Mutation | ACC,GCC | T68A | NP_001304926.1 |
| NM_032307.4 | 867 | Missense Mutation | ACC,GCC | T209A | NP_115683.3 |
| XM_005252271.4 | 867 | Intron | XP_005252328.1 |