| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001193503.1 | 580 | Intron | NP_001180432.1 | ||
| NM_001976.4 | 580 | Intron | NP_001967.3 | ||
| NM_053013.3 | 580 | Intron | NP_443739.3 | ||
| XM_005256521.2 | 580 | Missense Mutation | ACG,ATG | T28M | XP_005256578.1 |
| XM_011523729.1 | 580 | Missense Mutation | ACG,ATG | T19M | XP_011522031.1 |
| XM_017024346.1 | 580 | Missense Mutation | ACG,ATG | T19M | XP_016879835.1 |