| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001288983.1 | 2138 | Intron | NP_001275912.1 | ||
| NM_001288984.1 | 2138 | Intron | NP_001275913.1 | ||
| NM_018115.3 | 2138 | Intron | NP_060585.2 | ||
| XM_005263102.4 | 2138 | Missense Mutation | ACG,ATG | T629M | XP_005263159.1 |
| XM_005263105.4 | 2138 | Intron | XP_005263162.1 | ||
| XM_017008354.1 | 2138 | Intron | XP_016863843.1 | ||
| XM_017008355.1 | 2138 | Intron | XP_016863844.1 |