| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142777.1 | 641 | Intron | NP_001136249.1 | ||
| NM_001142778.1 | 641 | Intron | NP_001136250.1 | ||
| NM_025193.3 | 641 | Missense Mutation | CGT,TGT | R179C | NP_079469.2 |
| XM_005255601.3 | 641 | Missense Mutation | CGT,TGT | R179C | XP_005255658.2 |
| XM_011545960.2 | 641 | Missense Mutation | CGT,TGT | R179C | XP_011544262.1 |
| XM_011545961.1 | 641 | Missense Mutation | CGT,TGT | R179C | XP_011544263.1 |
| XM_011545962.2 | 641 | Intron | XP_011544264.1 | ||
| XM_017023732.1 | 641 | Intron | XP_016879221.1 |