| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_052947.3 | 5667 | Missense Mutation | ACT,ATT | T2112I | NP_443179.3 |
| XM_011525801.2 | 5667 | UTR 3 | XP_011524103.1 | ||
| XM_011525802.2 | 5667 | Missense Mutation | ACT,ATT | T2018I | XP_011524104.1 |
| XM_017025535.1 | 5667 | Intron | XP_016881024.1 | ||
| XM_017025536.1 | 5667 | Intron | XP_016881025.1 | ||
| XM_017025537.1 | 5667 | Intron | XP_016881026.1 | ||
| XM_017025538.1 | 5667 | Missense Mutation | ACT,ATT | T1443I | XP_016881027.1 |
| XM_017025539.1 | 5667 | Missense Mutation | ACT,ATT | T1443I | XP_016881028.1 |