| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142569.2 | 101 | Intron | NP_001136041.1 | ||
| NM_018265.3 | 101 | Missense Mutation | GCT,GTT | A34V | NP_060735.3 |
| XM_011509754.2 | 101 | Intron | XP_011508056.1 | ||
| XM_011509755.1 | 101 | Intron | XP_011508057.1 | ||
| XM_011509756.2 | 101 | Missense Mutation | GCT,GTT | A34V | XP_011508058.1 |