| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142883.1 | 1523 | Missense Mutation | CGC,TGC | R366C | NP_001136355.1 |
| NM_054111.4 | 1523 | Missense Mutation | CGC,TGC | R366C | NP_473452.2 |
| XM_005248842.3 | 1523 | Missense Mutation | CGC,TGC | R366C | XP_005248899.1 |
| XM_005248843.3 | 1523 | Missense Mutation | CGC,TGC | R253C | XP_005248900.1 |
| XM_011514295.2 | 1523 | Intron | XP_011512597.1 |