| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001281450.1 | 1210 | Missense Mutation | CGC,TGC | R361C | NP_001268379.1 |
| NM_001281451.1 | 1210 | Missense Mutation | CGC,TGC | R362C | NP_001268380.1 |
| NM_178125.3 | 1210 | Missense Mutation | CGC,TGC | R362C | NP_835226.2 |
| XM_011515787.1 | 1210 | Intron | XP_011514089.1 | ||
| XM_011515788.2 | 1210 | Missense Mutation | CGC,TGC | R153C | XP_011514090.1 |
| XM_011515789.2 | 1210 | Missense Mutation | CGC,TGC | R361C | XP_011514091.2 |