| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282856.1 | 5072 | Missense Mutation | ATC,TTC | I1645F | NP_001269785.1 |
| NM_001282858.1 | 5072 | Missense Mutation | ATC,TTC | I1645F | NP_001269787.1 |
| NM_001282860.1 | 5072 | Missense Mutation | ATC,TTC | I1645F | NP_001269789.1 |
| NM_001282861.1 | 5072 | Intron | NP_001269790.1 | ||
| NM_032292.5 | 5072 | Intron | NP_115668.4 | ||
| XM_005245284.3 | 5072 | Missense Mutation | ATC,TTC | I1473F | XP_005245341.1 |
| XM_005245286.3 | 5072 | Missense Mutation | ATC,TTC | I841F | XP_005245343.1 |
| XM_006711393.3 | 5072 | Missense Mutation | ATC,TTC | I1645F | XP_006711456.1 |
| XM_006711394.3 | 5072 | Missense Mutation | ATC,TTC | I1645F | XP_006711457.1 |
| XM_011509658.2 | 5072 | Missense Mutation | ATC,TTC | I1616F | XP_011507960.1 |
| XM_011509659.2 | 5072 | Missense Mutation | ATC,TTC | I1473F | XP_011507961.1 |