| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001270367.1 | 216 | Missense Mutation | CCC,CTC | P41L | NP_001257296.1 |
| NM_001270368.1 | 216 | Missense Mutation | CCC,CTC | P41L | NP_001257297.1 |
| NM_001270369.1 | 216 | Missense Mutation | CCC,CTC | P41L | NP_001257298.1 |
| NM_001270370.1 | 216 | Intron | NP_001257299.1 | ||
| NM_001270371.1 | 216 | Intron | NP_001257300.1 | ||
| NM_001270372.1 | 216 | Intron | NP_001257301.1 | ||
| NM_001270373.1 | 216 | Intron | NP_001257302.1 | ||
| NM_001270374.1 | 216 | Intron | NP_001257303.1 | ||
| NM_025125.3 | 216 | Intron | NP_079401.2 | ||
| XM_006717978.2 | 216 | Intron | XP_006718041.1 | ||
| XM_011540192.2 | 216 | Missense Mutation | CCC,CTC | P41L | XP_011538494.1 |
| XM_011540193.2 | 216 | Intron | XP_011538495.1 | ||
| XM_017016679.1 | 216 | Missense Mutation | CCC,CTC | P41L | XP_016872168.1 |
| XM_017016680.1 | 216 | Intron | XP_016872169.1 |