| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001347.3 | 2665 | Missense Mutation | AGA,GGA | R868G | NP_001338.2 |
| XM_011513411.1 | 2665 | Missense Mutation | AGA,GGA | R868G | XP_011511713.1 |
| XM_011513412.1 | 2665 | Intron | XP_011511714.1 | ||
| XM_011513414.2 | 2665 | Intron | XP_011511716.1 | ||
| XM_011513415.1 | 2665 | Intron | XP_011511717.1 | ||
| XM_017007814.1 | 2665 | Intron | XP_016863303.1 | ||
| XM_017007815.1 | 2665 | Intron | XP_016863304.1 |