| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014423.3 | 3938 | Missense Mutation | CGC,TGC | R1156C | NP_055238.1 |
| XM_005271963.4 | 3938 | Missense Mutation | CGC,TGC | R1156C | XP_005272020.1 |
| XM_005271964.4 | 3938 | Missense Mutation | CGC,TGC | R778C | XP_005272021.1 |
| XM_006714587.3 | 3938 | Missense Mutation | CGC,TGC | R1127C | XP_006714650.1 |