| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001244606.1 | 636 | Silent Mutation | CCA,CCG | P169P | NP_001231535.1 |
| NM_032549.3 | 636 | Silent Mutation | CCA,CCG | P169P | NP_115938.1 |
| XM_005250630.3 | 636 | Silent Mutation | CCA,CCG | P169P | XP_005250687.1 |
| XM_011516605.2 | 636 | Silent Mutation | CCA,CCG | P197P | XP_011514907.1 |
| XM_011516608.2 | 636 | Intron | XP_011514910.1 | ||
| XM_011516609.2 | 636 | UTR 3 | XP_011514911.1 | ||
| XM_011516611.2 | 636 | Intron | XP_011514913.1 | ||
| XM_011516613.2 | 636 | UTR 3 | XP_011514915.1 | ||
| XM_017012699.1 | 636 | Intron | XP_016868188.1 | ||
| XM_017012700.1 | 636 | Intron | XP_016868189.1 | ||
| XM_017012701.1 | 636 | Intron | XP_016868190.1 | ||
| XM_017012702.1 | 636 | Intron | XP_016868191.1 | ||
| XM_017012703.1 | 636 | Intron | XP_016868192.1 | ||
| XM_017012704.1 | 636 | Intron | XP_016868193.1 | ||
| XM_017012705.1 | 636 | Silent Mutation | CCA,CCG | P169P | XP_016868194.1 |