| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_024753.4 | 3999 | Missense Mutation | ACT,GCT | T1298A | NP_079029.3 |
| XM_006712761.1 | 3999 | Intron | XP_006712824.1 | ||
| XM_011511871.2 | 3999 | Missense Mutation | ACT,GCT | T1048A | XP_011510173.1 |
| XM_011511872.2 | 3999 | UTR 3 | XP_011510174.1 | ||
| XM_017004967.1 | 3999 | Intron | XP_016860456.1 | ||
| XM_017004968.1 | 3999 | Missense Mutation | ACT,GCT | T1080A | XP_016860457.1 |
| XM_017004969.1 | 3999 | Missense Mutation | ACT,GCT | T965A | XP_016860458.1 |