| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001040462.2 | 325 | Missense Mutation | CGC,TGC | R96C | NP_001035552.1 |
| NM_001159707.1 | 325 | Intron | NP_001153179.1 | ||
| NM_001159708.1 | 325 | Missense Mutation | CGC,TGC | R96C | NP_001153180.1 |
| NM_001159709.1 | 325 | Intron | NP_001153181.1 | ||
| NM_001159710.1 | 325 | Intron | NP_001153182.1 | ||
| NM_024850.2 | 325 | Missense Mutation | CGC,TGC | R96C | NP_079126.1 |
| XM_011534649.1 | 325 | Missense Mutation | CGC,TGC | R96C | XP_011532951.1 |
| XM_011534650.2 | 325 | Missense Mutation | CGC,TGC | R46C | XP_011532952.1 |
| XM_011534651.2 | 325 | Intron | XP_011532953.1 | ||
| XM_011534652.2 | 325 | Intron | XP_011532954.1 | ||
| XM_011534653.2 | 325 | Intron | XP_011532955.1 |