| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001098173.1 | 1073 | Missense Mutation | ACC,TCC | T292S | NP_001091643.1 |
| XM_005256274.3 | 1073 | Missense Mutation | ACC,TCC | T292S | XP_005256331.1 |
| XM_011522829.1 | 1073 | Missense Mutation | ACC,TCC | T292S | XP_011521131.1 |
| XM_011522831.2 | 1073 | Intron | XP_011521133.1 | ||
| XM_017022882.1 | 1073 | Intron | XP_016878371.1 | ||
| XM_017022883.1 | 1073 | Intron | XP_016878372.1 | ||
| XM_017022884.1 | 1073 | Intron | XP_016878373.1 |