| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001080493.3 | 382 | Missense Mutation | ATC,GTC | I107V | NP_001073962.1 |
| NM_001297610.1 | 382 | UTR 5 | NP_001284539.1 | ||
| NM_017507.1 | 382 | Missense Mutation | ATC,GTC | I63V | NP_059977.1 |
| XM_017026941.1 | 382 | UTR 5 | XP_016882430.1 | ||
| XM_017026942.1 | 382 | UTR 5 | XP_016882431.1 |