| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_006426.2 | 30 | Missense Mutation | ATC,TTC | I9F | NP_006417.2 |
| XM_005252658.3 | 30 | Intron | XP_005252715.1 | ||
| XM_011539125.2 | 30 | UTR 5 | XP_011537427.1 | ||
| XM_017015482.1 | 30 | Intron | XP_016870971.1 | ||
| XM_017015483.1 | 30 | Intron | XP_016870972.1 |