| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_016234.3 | 236 | Missense Mutation | GCG,TCG | A42S | NP_057318.2 |
| NM_203379.1 | 236 | Intron | NP_976313.1 | ||
| NM_203380.1 | 236 | Intron | NP_976314.1 | ||
| XM_017016324.1 | 236 | Missense Mutation | GCG,TCG | A42S | XP_016871813.1 |