ENST00000261937.11:c.4044C>G
MANE Select
|
ENSP00000261937.6:p.His1348Gln
|
|
ENST00000261937.10:c.4044C>G
|
ENSP00000261937.6:p.His1348Gln
|
|
ENST00000502603.5:n.744C>G
|
|
|
NM_182925.4:c.4044C>G
|
NP_891555.2:p.His1348Gln
|
|
XM_011534477.1:c.4293C>G
|
XP_011532779.1:p.His1431Gln
|
|
XM_011534478.1:c.4275C>G
|
XP_011532780.1:p.His1425Gln
|
|
XM_011534482.1:c.4062C>G
|
XP_011532784.1:p.His1354Gln
|
|
XM_011534483.1:c.3984C>G
|
XP_011532785.1:p.His1328Gln
|
|
XM_011534484.1:c.3585C>G
|
XP_011532786.1:p.His1195Gln
|
|
XR_941095.1:n.4330C>G
|
|
|
XM_011534478.3:c.4275C>G
|
XP_011532780.1:p.His1425Gln
|
|
XM_011534484.2:c.3585C>G
|
XP_011532786.1:p.His1195Gln
|
|
XM_017009263.1:c.*190C>G
|
XP_016864752.1:n.*190C>G
|
|
XM_017009268.1:c.3966C>G
|
XP_016864757.1:p.His1322Gln
|
|
XR_001742050.2:n.4534C>G
|
|
|
NM_182925.5:c.4044C>G
MANE Select
|
NP_891555.2:p.His1348Gln
|
|