| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001135821.1 | 361 | Missense Mutation | CGC,TGC | R48C | NP_001129293.1 |
| NM_001135822.1 | 361 | Intron | NP_001129294.1 | ||
| NM_001242824.1 | 361 | Intron | NP_001229753.1 | ||
| NM_001242825.1 | 361 | Intron | NP_001229754.1 | ||
| NM_002004.3 | 361 | Missense Mutation | CGC,TGC | R48C | NP_001995.1 |
| XM_005244962.1 | 361 | Intron | XP_005245019.1 | ||
| XM_005244963.1 | 361 | Intron | XP_005245020.1 |