| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001252195.1 | 271 | Intron | NP_001239124.1 | ||
| NM_032596.3 | 271 | Missense Mutation | TCC,TGC | S18C | NP_115985.2 |
| NM_147168.1 | 271 | Intron | NP_671697.1 | ||
| NM_147169.2 | 271 | Intron | NP_671698.1 | ||
| XM_005251616.4 | 271 | Missense Mutation | TCC,TGC | S18C | XP_005251673.1 |
| XM_005251618.4 | 271 | Intron | XP_005251675.1 | ||
| XM_011518055.2 | 271 | Intron | XP_011516357.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001184940.1 | 271 | Intron | NP_001171869.1 | ||
| NM_001184941.1 | 271 | Intron | NP_001171870.1 | ||
| NM_001184942.1 | 271 | Intron | NP_001171871.1 | ||
| NM_001184943.1 | 271 | Intron | NP_001171872.1 | ||
| NM_001184945.1 | 271 | Intron | NP_001171874.1 | ||
| NM_147202.1 | 271 | Intron | NP_671735.1 | ||
| XM_005251402.4 | 271 | Intron | XP_005251459.1 | ||
| XM_011517797.2 | 271 | Intron | XP_011516099.1 | ||
| XM_011517798.2 | 271 | Intron | XP_011516100.1 | ||
| XM_011517799.2 | 271 | Intron | XP_011516101.1 |