| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003447.3 | 237 | Missense Mutation | CGC,TGC | R69C | NP_003438.1 |
| XM_017011258.1 | 237 | Missense Mutation | CGC,TGC | R69C | XP_016866747.1 |
| XM_017011259.1 | 237 | Missense Mutation | CGC,TGC | R69C | XP_016866748.1 |
| XM_017011260.1 | 237 | Missense Mutation | CGC,TGC | R69C | XP_016866749.1 |
| XM_017011261.1 | 237 | Intron | XP_016866750.1 | ||
| XM_017011262.1 | 237 | Missense Mutation | CGC,TGC | R69C | XP_016866751.1 |