| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000167.5 | 223 | Missense Mutation | GCG,GTG | A15V | NP_000158.1 |
| NM_001128127.2 | 223 | Missense Mutation | GCG,GTG | A15V | NP_001121599.1 |
| NM_001205019.1 | 223 | Missense Mutation | GCG,GTG | A15V | NP_001191948.1 |
| NM_203391.3 | 223 | Missense Mutation | GCG,GTG | A15V | NP_976325.1 |
| XM_005274488.4 | 223 | Intron | XP_005274545.1 | ||
| XM_006724483.2 | 223 | Intron | XP_006724546.1 | ||
| XM_006724484.2 | 223 | Intron | XP_006724547.1 | ||
| XM_006724485.2 | 223 | Intron | XP_006724548.1 | ||
| XM_006724486.3 | 223 | Intron | XP_006724549.1 | ||
| XM_011545491.2 | 223 | Intron | XP_011543793.1 | ||
| XM_011545492.1 | 223 | Intron | XP_011543794.1 | ||
| XM_011545493.2 | 223 | Intron | XP_011543795.1 | ||
| XM_011545494.2 | 223 | Intron | XP_011543796.1 | ||
| XM_017029409.1 | 223 | Intron | XP_016884898.1 | ||
| XM_017029410.1 | 223 | Intron | XP_016884899.1 | ||
| XM_017029411.1 | 223 | Intron | XP_016884900.1 | ||
| XM_017029412.1 | 223 | Intron | XP_016884901.1 |