| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001321768.1 | 219 | Intron | NP_001308697.1 | ||
| NM_020813.3 | 219 | Missense Mutation | CAA,CTA | Q29L | NP_065864.2 |
| XM_011527148.1 | 219 | Missense Mutation | CAA,CTA | Q29L | XP_011525450.1 |
| XM_017027032.1 | 219 | Intron | XP_016882521.1 |