| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001127182.1 | 383 | Missense Mutation | ACA,GCA | T26A | NP_001120654.1 |
| NM_018131.4 | 383 | Missense Mutation | ACA,GCA | T26A | NP_060601.3 |
| XM_011539918.1 | 383 | UTR 5 | XP_011538220.1 | ||
| XM_011539919.1 | 383 | Intron | XP_011538221.1 | ||
| XM_011539920.2 | 383 | Intron | XP_011538222.1 | ||
| XM_017016372.1 | 383 | Intron | XP_016871861.1 | ||
| XM_017016373.1 | 383 | Intron | XP_016871862.1 |