| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001146702.1 | 4688 | Intron | NP_001140174.1 | ||
| NM_001282622.1 | 4688 | Nonsense Mutation | CGA,TGA | R1473* | NP_001269551.1 |
| NM_004187.3 | 4688 | Nonsense Mutation | CGA,TGA | R1474* | NP_004178.2 |
| XM_005262035.4 | 4688 | Nonsense Mutation | CGA,TGA | R1471* | XP_005262092.1 |
| XM_011530824.2 | 4688 | Nonsense Mutation | CGA,TGA | R1448* | XP_011529126.1 |
| XM_011530825.2 | 4688 | Nonsense Mutation | CGA,TGA | R1433* | XP_011529127.1 |
| XM_011530826.2 | 4688 | Nonsense Mutation | CGA,TGA | R1430* | XP_011529128.1 |
| XM_011530827.2 | 4688 | Intron | XP_011529129.1 | ||
| XM_011530828.1 | 4688 | Intron | XP_011529130.1 | ||
| XM_011530829.2 | 4688 | Nonsense Mutation | CGA,TGA | R1309* | XP_011529131.1 |
| XM_011530830.2 | 4688 | Nonsense Mutation | CGA,TGA | R1309* | XP_011529132.1 |
| XM_011530831.2 | 4688 | Nonsense Mutation | CGA,TGA | R1146* | XP_011529133.1 |
| XM_017029886.1 | 4688 | Intron | XP_016885375.1 | ||
| XM_017029887.1 | 4688 | Intron | XP_016885376.1 | ||
| XM_017029888.1 | 4688 | Intron | XP_016885377.1 | ||
| XM_017029889.1 | 4688 | Intron | XP_016885378.1 |