| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_018666.2 | 977 | Missense Mutation | ATC,TTC | I268F | NP_061136.2 |
| XM_017029621.1 | 977 | Missense Mutation | ATC,TTC | I268F | XP_016885110.1 |
| XM_017029622.1 | 977 | Intron | XP_016885111.1 | ||
| XM_017029623.1 | 977 | Missense Mutation | ATC,TTC | I268F | XP_016885112.1 |
| XM_017029624.1 | 977 | Missense Mutation | ATC,TTC | I237F | XP_016885113.1 |
| XM_017029625.1 | 977 | Missense Mutation | ATC,TTC | I268F | XP_016885114.1 |
| XM_017029626.1 | 977 | Missense Mutation | ATC,TTC | I29F | XP_016885115.1 |
| XM_017029627.1 | 977 | Intron | XP_016885116.1 |