| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_182833.1 | 2140 | UTR 3 | NP_878253.1 | ||
| XM_011544826.1 | 2140 | UTR 3 | XP_011543128.1 | ||
| XM_011544833.1 | 2140 | Intron | XP_011543135.1 | ||
| XM_011544834.1 | 2140 | Missense Mutation | CCA,TCA | P581S | XP_011543136.1 |
| XM_017017348.1 | 2140 | Intron | XP_016872837.1 | ||
| XM_017017349.1 | 2140 | Intron | XP_016872838.1 | ||
| XM_017017350.1 | 2140 | Intron | XP_016872839.1 | ||
| XM_017017351.1 | 2140 | Intron | XP_016872840.1 |