| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001081676.1 | 6496 | Missense Mutation | AGT,TGT | S1912C | NP_001075145.1 |
| NM_001081677.1 | 6496 | Missense Mutation | AGT,TGT | S1912C | NP_001075146.1 |
| NM_006922.3 | 6496 | Missense Mutation | AGT,TGT | S1961C | NP_008853.3 |
| XM_011511610.2 | 6496 | Missense Mutation | AGT,TGT | S1961C | XP_011509912.1 |
| XM_011511613.2 | 6496 | Missense Mutation | AGT,TGT | S1331C | XP_011509915.1 |
| XM_017004660.1 | 6496 | Missense Mutation | AGT,TGT | S1961C | XP_016860149.1 |
| XM_017004661.1 | 6496 | Missense Mutation | AGT,TGT | S1944C | XP_016860150.1 |
| XM_017004662.1 | 6496 | Missense Mutation | AGT,TGT | S1915C | XP_016860151.1 |
| XM_017004663.1 | 6496 | Missense Mutation | AGT,TGT | S1331C | XP_016860152.1 |
| XM_017004664.1 | 6496 | Intron | XP_016860153.1 | ||
| XM_017004665.1 | 6496 | Intron | XP_016860154.1 | ||
| XM_017004666.1 | 6496 | Intron | XP_016860155.1 |