| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_138383.2 | 2203 | Missense Mutation | GCC,GTC | A577V | NP_612392.1 |
| XM_005256236.4 | 2203 | Missense Mutation | GCC,GTC | A675V | XP_005256293.2 |
| XM_011523450.2 | 2203 | Missense Mutation | GCC,GTC | A621V | XP_011521752.1 |
| XM_011523453.2 | 2203 | Missense Mutation | GCC,GTC | A729V | XP_011521755.2 |
| XM_011523454.2 | 2203 | Missense Mutation | GCC,GTC | A726V | XP_011521756.2 |
| XM_011523458.2 | 2203 | Missense Mutation | GCC,GTC | A448V | XP_011521760.1 |
| XM_017023879.1 | 2203 | Missense Mutation | GCC,GTC | A697V | XP_016879368.1 |
| XM_017023880.1 | 2203 | Missense Mutation | GCC,GTC | A685V | XP_016879369.1 |
| XM_017023881.1 | 2203 | Missense Mutation | GCC,GTC | A678V | XP_016879370.1 |
| XM_017023882.1 | 2203 | Intron | XP_016879371.1 | ||
| XM_017023883.1 | 2203 | Intron | XP_016879372.1 | ||
| XM_017023884.1 | 2203 | Intron | XP_016879373.1 |