| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001279356.1 | 577 | Intron | NP_001266285.1 | ||
| NM_001279357.1 | 577 | Intron | NP_001266286.1 | ||
| NM_001279358.1 | 577 | Intron | NP_001266287.1 | ||
| NM_001279359.1 | 577 | Intron | NP_001266288.1 | ||
| NM_001279360.1 | 577 | Intron | NP_001266289.1 | ||
| NM_006330.3 | 577 | Intron | NP_006321.1 | ||
| XM_005251127.4 | 577 | Missense Mutation | CCA,GCA | P146A | XP_005251184.1 |
| XM_017012956.1 | 577 | Intron | XP_016868445.1 | ||
| XM_017012957.1 | 577 | Intron | XP_016868446.1 | ||
| XM_017012958.1 | 577 | Intron | XP_016868447.1 | ||
| XM_017012959.1 | 577 | Intron | XP_016868448.1 | ||
| XM_017012960.1 | 577 | Intron | XP_016868449.1 |