| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001318372.1 | 4322 | Missense Mutation | CAA,CAC | Q1168H | NP_001305301.1 |
| NM_001318373.1 | 4322 | Missense Mutation | CAA,CAC | Q1134H | NP_001305302.1 |
| NM_001318374.1 | 4322 | Intron | NP_001305303.1 | ||
| NM_020403.4 | 4322 | Missense Mutation | CAA,CAC | Q1176H | NP_065136.1 |
| NM_203487.2 | 4322 | Missense Mutation | CAA,CAC | Q1210H | NP_982354.1 |
| XM_005266408.3 | 4322 | Intron | XP_005266465.1 | ||
| XM_011535099.2 | 4322 | Intron | XP_011533401.1 | ||
| XM_017020619.1 | 4322 | Missense Mutation | CAA,CAC | Q1210H | XP_016876108.1 |
| XM_017020620.1 | 4322 | Intron | XP_016876109.1 | ||
| XM_017020621.1 | 4322 | Intron | XP_016876110.1 |