| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001300800.1 | 20 | Intron | NP_001287729.1 | ||
| NM_024771.3 | 20 | UTR 5 | NP_079047.2 | ||
| XM_006718689.3 | 20 | UTR 5 | XP_006718752.1 | ||
| XM_011545254.2 | 20 | Missense Mutation | CCC,CGC | P2R | XP_011543556.1 |
| XM_011545255.2 | 20 | Missense Mutation | CCC,CGC | P2R | XP_011543557.1 |