| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_004985.4 | 688 | Intron | NP_004976.2 | ||
| NM_033360.3 | 688 | Nonsense Mutation | CGA,TGA | R164* | NP_203524.1 |
| XM_006719069.3 | 688 | Nonsense Mutation | CGA,TGA | R164* | XP_006719132.1 |
| XM_011520653.2 | 688 | Intron | XP_011518955.1 | ||
| XM_017019292.1 | 688 | Intron | XP_016874781.1 | ||
| XM_017019293.1 | 688 | Nonsense Mutation | CGA,TGA | R164* | XP_016874782.1 |