| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001040697.2 | 758 | Missense Mutation | ACC,ATC | T442I | NP_001035787.1 |
| NM_001261382.1 | 758 | Missense Mutation | ACC,ATC | T420I | NP_001248311.1 |
| NM_001261383.1 | 758 | UTR 3 | NP_001248312.1 | ||
| NM_001261384.1 | 758 | Missense Mutation | ACC,ATC | T312I | NP_001248313.1 |
| NM_001261385.1 | 758 | UTR 3 | NP_001248314.1 | ||
| NM_001261386.1 | 758 | UTR 3 | NP_001248315.1 | ||
| NM_001297771.1 | 758 | Intron | NP_001284700.1 | ||
| NM_018314.4 | 758 | UTR 3 | NP_060784.3 | ||
| XM_006718255.2 | 758 | Missense Mutation | ACC,ATC | T219I | XP_006718318.1 |
| XM_011520201.2 | 758 | Missense Mutation | ACC,ATC | T219I | XP_011518503.1 |
| XM_017017985.1 | 758 | Missense Mutation | ACC,ATC | T312I | XP_016873474.1 |
| XM_017017986.1 | 758 | UTR 3 | XP_016873475.1 |