| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001195194.1 | 894 | Intron | NP_001182123.1 | ||
| NM_001195195.1 | 894 | Intron | NP_001182124.1 | ||
| NM_001251964.1 | 894 | Missense Mutation | CAT,CGT | H71R | NP_001238893.1 |
| NM_022112.2 | 894 | Intron | NP_071395.2 | ||
| XM_017018113.1 | 894 | Intron | XP_016873602.1 | ||
| XM_017018114.1 | 894 | Intron | XP_016873603.1 | ||
| XM_017018115.1 | 894 | Intron | XP_016873604.1 | ||
| XM_017018116.1 | 894 | Intron | XP_016873605.1 | ||
| XM_017018117.1 | 894 | Intron | XP_016873606.1 |