| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015653.4 | 386 | Missense Mutation | GCC,GGC | A122G | NP_056468.3 |
| XM_005261524.4 | 386 | Missense Mutation | GCC,GGC | A49G | XP_005261581.1 |
| XM_011530126.2 | 386 | Intron | XP_011528428.1 | ||
| XM_017028766.1 | 386 | Missense Mutation | GCC,GGC | A122G | XP_016884255.1 |