| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001130111.1 | 5262 | Intron | NP_001123583.1 | ||
| NM_031213.3 | 5262 | Intron | NP_112490.3 | ||
| XM_011528338.1 | 5262 | Missense Mutation | ATC,GTC | I294V | XP_011526640.1 |
| XM_017027341.1 | 5262 | Missense Mutation | ATC,GTC | I243V | XP_016882830.1 |
| XM_017027342.1 | 5262 | Missense Mutation | ATC,GTC | I95V | XP_016882831.1 |