| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_016233.2 | 89 | Missense Mutation | CCG,GCG | P17A | NP_057317.2 |
| XM_011541571.2 | 89 | Intron | XP_011539873.1 | ||
| XM_011541572.2 | 89 | Missense Mutation | CCG,GCG | P17A | XP_011539874.1 |
| XM_017001463.1 | 89 | Intron | XP_016856952.1 |