| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001302961.1 | 697 | Missense Mutation | NP_001289890.1 | ||
| NM_004917.4 | 697 | Missense Mutation | NP_004908.4 | ||
| XM_005259441.4 | 697 | Missense Mutation | XP_005259498.2 | ||
| XM_011527545.2 | 697 | Intron | XP_011525847.1 | ||
| XM_011527546.2 | 697 | UTR 3 | XP_011525848.1 |