| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001137605.2 | 78 | UTR 5 | NP_001131077.1 | ||
| NM_022141.6 | 78 | Intron | NP_071424.1 | ||
| XM_005261702.3 | 78 | Intron | XP_005261759.1 | ||
| XM_011530302.2 | 78 | Missense Mutation | CGT,TGT | R11C | XP_011528604.1 |
| XM_017028907.1 | 78 | Intron | XP_016884396.1 | ||
| XM_017028908.1 | 78 | Intron | XP_016884397.1 |