| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001017397.1 | 2428 | Intron | NP_001017397.1 | ||
| NM_001017398.1 | 2428 | Intron | NP_001017398.1 | ||
| NM_001300752.1 | 2428 | Missense Mutation | GCT,GTT | A481V | NP_001287681.1 |
| NM_001300759.1 | 2428 | Missense Mutation | GCT,GTT | A624V | NP_001287688.1 |
| NM_018700.3 | 2428 | Missense Mutation | GCT,GTT | A636V | NP_061170.2 |
| XM_017009621.1 | 2428 | Missense Mutation | GCT,GTT | A653V | XP_016865110.1 |
| XM_017009622.1 | 2428 | Missense Mutation | GCT,GTT | A641V | XP_016865111.1 |
| XM_017009623.1 | 2428 | Intron | XP_016865112.1 |