| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001077186.1 | 22 | Intron | NP_001070654.1 | ||
| NM_001145809.1 | 22 | Intron | NP_001139281.1 | ||
| NM_024729.3 | 22 | Intron | NP_079005.3 | ||
| XM_006723386.3 | 22 | Intron | XP_006723449.1 | ||
| XM_011527320.2 | 22 | Missense Mutation | CAA,CGA | Q6R | XP_011525622.1 |
| XM_011527321.2 | 22 | Missense Mutation | CAA,CGA | Q6R | XP_011525623.1 |
| XM_011527323.2 | 22 | Intron | XP_011525625.1 |