| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282195.1 | 291 | Missense Mutation | ACG,GCG | T19A | NP_001269124.1 |
| NM_001282196.1 | 291 | Missense Mutation | ACG,GCG | T19A | NP_001269125.1 |
| NM_001282197.1 | 291 | Missense Mutation | ACG,GCG | T19A | NP_001269126.1 |
| NM_001282198.1 | 291 | Intron | NP_001269127.1 | ||
| XM_005262489.4 | 291 | Intron | XP_005262546.1 | ||
| XM_011531402.2 | 291 | Missense Mutation | ACG,GCG | T19A | XP_011529704.1 |
| XM_011531403.1 | 291 | Intron | XP_011529705.1 | ||
| XM_017029936.1 | 291 | Intron | XP_016885425.1 | ||
| XM_017029937.1 | 291 | Missense Mutation | ACG,GCG | T19A | XP_016885426.1 |
| XM_017029938.1 | 291 | Missense Mutation | ACG,GCG | T19A | XP_016885427.1 |
| XM_017029939.1 | 291 | Missense Mutation | ACG,GCG | T19A | XP_016885428.1 |
| XM_017029940.1 | 291 | Intron | XP_016885429.1 | ||
| XM_017029941.1 | 291 | UTR 5 | XP_016885430.1 | ||
| XM_017029942.1 | 291 | Intron | XP_016885431.1 | ||
| XM_017029943.1 | 291 | Intron | XP_016885432.1 |