| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001135175.1 | 334 | Missense Mutation | GCA,TCA | A6S | NP_001128647.1 |
| NM_001135176.1 | 334 | UTR 5 | NP_001128648.1 | ||
| NM_001135177.1 | 334 | Intron | NP_001128649.1 | ||
| NM_152905.3 | 334 | UTR 5 | NP_690869.1 | ||
| XM_005268644.2 | 334 | Missense Mutation | GCA,TCA | A6S | XP_005268701.1 |
| XM_006719237.3 | 334 | Intron | XP_006719300.1 | ||
| XM_011537903.2 | 334 | Intron | XP_011536205.1 | ||
| XM_011537904.2 | 334 | UTR 5 | XP_011536206.1 | ||
| XM_011537905.2 | 334 | Intron | XP_011536207.1 | ||
| XM_011537906.2 | 334 | Intron | XP_011536208.1 | ||
| XM_017018801.1 | 334 | Intron | XP_016874290.1 | ||
| XM_017018802.1 | 334 | Intron | XP_016874291.1 |