| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001129996.1 | 192 | Intron | NP_001123468.1 | ||
| NM_013360.2 | 192 | Missense Mutation | GCA,TCA | A2S | NP_037492.2 |
| XM_005259208.3 | 192 | Missense Mutation | GCA,TCA | A2S | XP_005259265.1 |
| XM_005259209.3 | 192 | Intron | XP_005259266.1 | ||
| XM_017027237.1 | 192 | Intron | XP_016882726.1 | ||
| XM_017027238.1 | 192 | Missense Mutation | GCA,TCA | A2S | XP_016882727.1 |