| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001318029.1 | 427 | Missense Mutation | CTC,TTC | L37F | NP_001304958.1 |
| NM_176875.3 | 427 | Missense Mutation | CTC,TTC | L37F | NP_795344.1 |
| XM_005253210.1 | 427 | Missense Mutation | CTC,TTC | L37F | XP_005253267.1 |
| XM_017018516.1 | 427 | Intron | XP_016874005.1 |