| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001287516.1 | 980 | Intron | NP_001274445.1 | ||
| NM_001287517.1 | 980 | Intron | NP_001274446.1 | ||
| NM_001287518.1 | 980 | Intron | NP_001274447.1 | ||
| NM_001287519.1 | 980 | Intron | NP_001274448.1 | ||
| NM_001287520.1 | 980 | Intron | NP_001274449.1 | ||
| NM_001287522.1 | 980 | Intron | NP_001274451.1 | ||
| NM_001287524.1 | 980 | Intron | NP_001274453.1 | ||
| NM_004358.4 | 980 | Missense Mutation | ACC,GCC | T63A | NP_004349.1 |
| NM_021872.3 | 980 | Missense Mutation | ACC,GCC | T63A | NP_068658.1 |
| NM_021873.3 | 980 | Missense Mutation | ACC,GCC | T63A | NP_068659.1 |