| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001197301.1 | 354 | Intron | NP_001184230.1 | ||
| NM_001197302.1 | 354 | Intron | NP_001184231.1 | ||
| NM_014419.3 | 354 | Missense Mutation | GCG,GGG | A96G | NP_055234.1 |
| XM_006723142.2 | 354 | Missense Mutation | GCG,GGG | A111G | XP_006723205.1 |
| XM_011526724.1 | 354 | Missense Mutation | GCG,GGG | A119G | XP_011525026.1 |
| XM_011526725.1 | 354 | Missense Mutation | GCG,GGG | A103G | XP_011525027.1 |
| XM_011526726.2 | 354 | Missense Mutation | GCG,GGG | A103G | XP_011525028.1 |
| XM_011526727.2 | 354 | Missense Mutation | GCG,GGG | A119G | XP_011525029.1 |
| XM_011526728.2 | 354 | Intron | XP_011525030.1 | ||
| XM_011526729.1 | 354 | Missense Mutation | GCG,GGG | A21G | XP_011525031.1 |
| XM_017026593.1 | 354 | Missense Mutation | GCG,GGG | A21G | XP_016882082.1 |