| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001024924.1 | 279 | Missense Mutation | ACA,CCA | T41P | NP_001020095.1 |
| NM_018261.3 | 279 | Missense Mutation | ACA,CCA | T41P | NP_060731.2 |
| NM_178237.2 | 279 | Missense Mutation | ACA,CCA | T41P | NP_839955.1 |
| XM_005265747.2 | 279 | Missense Mutation | ACA,CCA | T41P | XP_005265804.1 |
| XM_005265748.1 | 279 | Missense Mutation | ACA,CCA | T41P | XP_005265805.1 |
| XM_005265750.2 | 279 | Missense Mutation | ACA,CCA | T41P | XP_005265807.1 |
| XM_017008405.1 | 279 | Missense Mutation | ACA,CCA | T41P | XP_016863894.1 |
| XM_017008406.1 | 279 | Missense Mutation | ACA,CCA | T41P | XP_016863895.1 |
| XM_017008407.1 | 279 | Missense Mutation | ACA,CCA | T41P | XP_016863896.1 |
| XM_017008408.1 | 279 | Intron | XP_016863897.1 | ||
| XM_017008409.1 | 279 | Intron | XP_016863898.1 |