Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000600.4 | 622 | Missense Mutation | CAA,CAC | Q56H | NP_000591.1 |
NM_001318095.1 | 622 | Intron | NP_001305024.1 | ||
XM_005249745.4 | 622 | Missense Mutation | CAA,CAC | Q110H | XP_005249802.1 |
XM_011515390.2 | 622 | Missense Mutation | CAA,CAC | Q56H | XP_011513692.1 |