| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001165881.2 | 382 | Nonsense Mutation | CGA,TGA | R18* | NP_001159353.1 |
| NM_001165882.2 | 382 | UTR 5 | NP_001159354.1 | ||
| NM_001165883.1 | 382 | Nonsense Mutation | CGA,TGA | R18* | NP_001159355.1 |
| NM_001165884.2 | 382 | Intron | NP_001159356.2 | ||
| NM_001165885.1 | 382 | Nonsense Mutation | CGA,TGA | R18* | NP_001159357.1 |
| NM_001165886.1 | 382 | Intron | NP_001159358.1 | ||
| NM_001165887.1 | 382 | Intron | NP_001159359.1 | ||
| NM_003415.2 | 382 | Nonsense Mutation | CGA,TGA | R18* | NP_003406.1 |
| NM_152943.2 | 382 | Nonsense Mutation | CGA,TGA | R18* | NP_694422.2 |