| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001193304.2 | 491 | Missense Mutation | CGC,TGC | R197C | NP_001180233.1 |
| NM_017849.3 | 491 | Missense Mutation | CGC,TGC | R197C | NP_060319.1 |
| XM_017004450.1 | 491 | UTR 5 | XP_016859939.1 | ||
| XM_017004451.1 | 491 | Missense Mutation | CGC,TGC | R113C | XP_016859940.1 |
| XM_017004452.1 | 491 | Missense Mutation | CGC,TGC | R113C | XP_016859941.1 |