| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001243963.1 | 2123 | Missense Mutation | CCA,TCA | P681S | NP_001230892.1 |
| NM_020871.3 | 2123 | Missense Mutation | CCA,TCA | P698S | NP_065922.3 |
| XM_006724724.3 | 2123 | Missense Mutation | CCA,TCA | P691S | XP_006724787.2 |
| XM_017029696.1 | 2123 | Intron | XP_016885185.1 | ||
| XM_017029697.1 | 2123 | Intron | XP_016885186.1 |