| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_153614.3 | 1169 | Missense Mutation | GCG,GTG | A54V | NP_705842.2 |
| XM_005273984.3 | 1169 | Missense Mutation | GCG,GTG | A54V | XP_005274041.1 |
| XM_011545004.2 | 1169 | Missense Mutation | GCG,GTG | A88V | XP_011543306.1 |
| XM_011545005.2 | 1169 | Missense Mutation | GCG,GTG | A88V | XP_011543307.1 |
| XM_011545007.2 | 1169 | UTR 5 | XP_011543309.1 | ||
| XM_011545009.2 | 1169 | UTR 5 | XP_011543311.1 | ||
| XM_011545013.2 | 1169 | Missense Mutation | GCG,GTG | A88V | XP_011543315.1 |
| XM_011545014.2 | 1169 | Missense Mutation | GCG,GTG | A88V | XP_011543316.1 |
| XM_011545015.2 | 1169 | Intron | XP_011543317.1 | ||
| XM_017017675.1 | 1169 | UTR 5 | XP_016873164.1 | ||
| XM_017017676.1 | 1169 | UTR 5 | XP_016873165.1 | ||
| XM_017017677.1 | 1169 | UTR 5 | XP_016873166.1 | ||
| XM_017017678.1 | 1169 | UTR 5 | XP_016873167.1 | ||
| XM_017017679.1 | 1169 | Missense Mutation | GCG,GTG | A88V | XP_016873168.1 |