| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001129888.1 | 844 | Intron | NP_001123360.1 | ||
| NM_032687.3 | 844 | Intron | NP_116076.1 | ||
| NM_138496.1 | 844 | Silent Mutation | CCA,CCG | P192P | NP_612505.1 |
| XM_006716560.3 | 844 | Intron | XP_006716623.1 | ||
| XM_006716561.3 | 844 | Intron | XP_006716624.1 | ||
| XM_006716562.3 | 844 | Silent Mutation | CCA,CCG | P234P | XP_006716625.2 |
| XM_011517051.1 | 844 | Silent Mutation | CCA,CCG | P104P | XP_011515353.1 |
| XM_017013463.1 | 844 | Silent Mutation | CCA,CCG | P141P | XP_016868952.1 |
| XM_017013464.1 | 844 | Silent Mutation | CCA,CCG | P141P | XP_016868953.1 |
| XM_017013465.1 | 844 | Silent Mutation | CCA,CCG | P141P | XP_016868954.1 |
| XM_017013466.1 | 844 | Silent Mutation | CCA,CCG | P141P | XP_016868955.1 |