| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001009814.1 | 5495 | Intron | NP_001009814.1 | ||
| NM_015058.1 | 5495 | Missense Mutation | ACA,GCA | T1809A | NP_055873.1 |
| XM_006719791.3 | 5495 | Missense Mutation | ACA,GCA | T1454A | XP_006719854.1 |
| XM_011535007.2 | 5495 | Intron | XP_011533309.1 | ||
| XM_017020469.1 | 5495 | Missense Mutation | ACA,GCA | T1748A | XP_016875958.1 |
| XM_017020470.1 | 5495 | Intron | XP_016875959.1 | ||
| XM_017020471.1 | 5495 | Intron | XP_016875960.1 | ||
| XM_017020472.1 | 5495 | Missense Mutation | ACA,GCA | T1063A | XP_016875961.1 |
| XM_017020473.1 | 5495 | Missense Mutation | ACA,GCA | T1046A | XP_016875962.1 |
| XM_017020474.1 | 5495 | Intron | XP_016875963.1 |