| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_018052.3 | 2567 | Missense Mutation | AAC,AGC | N770S | NP_060522.3 |
| XM_005256038.3 | 2567 | UTR 3 | XP_005256095.1 | ||
| XM_005256041.3 | 2567 | Intron | XP_005256098.2 | ||
| XM_011523223.2 | 2567 | Intron | XP_011521525.1 | ||
| XM_011523224.2 | 2567 | Intron | XP_011521526.1 | ||
| XM_011523225.2 | 2567 | Intron | XP_011521527.1 | ||
| XM_017023441.1 | 2567 | Intron | XP_016878930.1 | ||
| XM_017023442.1 | 2567 | Intron | XP_016878931.1 |