ENST00000358062.7:c.2166G>C
|
ENSP00000350765.3:p.Gln722His
|
|
ENST00000682238.1:c.-61G>C
|
ENSP00000508124.1:n.-61G>C
|
|
ENST00000683117.1:n.981G>C
|
|
|
ENST00000683450.1:n.903G>C
|
|
|
ENST00000683851.1:n.981G>C
|
|
|
ENST00000683957.1:n.812G>C
|
|
|
ENST00000684130.1:c.-61G>C
|
ENSP00000508037.1:n.-61G>C
|
|
ENST00000357033.9:c.7320G>C
MANE Select
|
ENSP00000354923.3:p.Gln2440His
|
|
ENST00000619831.5:c.3288G>C
|
ENSP00000479270.2:p.Gln1096His
|
|
ENST00000620040.5:c.-61G>C
|
ENSP00000478150.2:n.-61G>C
|
|
ENST00000680961.1:c.-61G>C
|
ENSP00000506386.1:n.-61G>C
|
|
ENST00000681646.1:n.981G>C
|
|
|
ENST00000681839.1:c.309G>C
|
ENSP00000505228.1:p.Gln103His
|
|
ENST00000357033.8:c.7320G>C
|
ENSP00000354923.3:p.Gln2440His
|
|
ENST00000358062.6:c.408G>C
|
ENSP00000350765.2:p.Gln136His
|
|
ENST00000359836.5:c.-61G>C
|
ENSP00000352894.1:n.-61G>C
|
|
ENST00000378677.6:c.7308G>C
|
ENSP00000367948.2:p.Gln2436His
|
|
ENST00000378707.7:c.-61G>C
|
ENSP00000367979.3:n.-61G>C
|
|
ENST00000471779.1:c.77G>C
|
ENSP00000417075.1:p.Arg26Thr
|
|
ENST00000474231.5:c.-61G>C
|
ENSP00000417123.1:n.-61G>C
|
|
ENST00000541735.5:c.-61G>C
|
ENSP00000444119.1:n.-61G>C
|
|
ENST00000619831.4:c.7305G>C
|
ENSP00000479270.1:p.Gln2435His
|
|
ENST00000620040.4:c.7317G>C
|
ENSP00000478150.1:p.Gln2439His
|
|
NM_000109.3:c.7296G>C
|
NP_000100.2:p.Gln2432His
|
|
NM_004006.2:c.7320G>C , LRG_199t1:c.7320G>C
|
NP_003997.1:p.Gln2440His
|
|
NM_004009.3:c.7308G>C
|
NP_004000.1:p.Gln2436His
|
|
NM_004010.3:c.6951G>C
|
NP_004001.1:p.Gln2317His
|
|
NM_004011.3:c.3297G>C
|
NP_004002.2:p.Gln1099His
|
|
NM_004012.3:c.3288G>C
|
NP_004003.1:p.Gln1096His
|
|
NM_004013.2:c.-61G>C
|
NP_004004.1:n.-61G>C
|
|
NM_004020.3:c.-61G>C
|
NP_004011.2:n.-61G>C
|
|
NM_004021.2:c.-61G>C
|
NP_004012.1:n.-61G>C
|
|
NM_004022.2:c.-61G>C
|
NP_004013.1:n.-61G>C
|
|
NM_004023.2:c.-61G>C
|
NP_004014.1:n.-61G>C
|
|
XM_006724468.2:c.7320G>C
|
XP_006724531.1:p.Gln2440His
|
|
XM_006724469.2:c.7296G>C
|
XP_006724532.1:p.Gln2432His
|
|
XM_006724470.2:c.7320G>C
|
XP_006724533.1:p.Gln2440His
|
|
XM_006724471.2:c.7320G>C
|
XP_006724534.1:p.Gln2440His
|
|
XM_006724472.2:c.7191G>C
|
XP_006724535.1:p.Gln2397His
|
|
XM_006724473.2:c.7182G>C
|
XP_006724536.1:p.Gln2394His
|
|
XM_006724474.2:c.7320G>C
|
XP_006724537.1:p.Gln2440His
|
|
XM_006724475.2:c.7320G>C
|
XP_006724538.1:p.Gln2440His
|
|
XM_011545467.1:c.7197G>C
|
XP_011543769.1:p.Gln2399His
|
|
XM_011545468.1:c.7320G>C
|
XP_011543770.1:p.Gln2440His
|
|
XM_006724469.3:c.7296G>C
|
XP_006724532.1:p.Gln2432His
|
|
XM_006724470.3:c.7320G>C
|
XP_006724533.1:p.Gln2440His
|
|
XM_006724474.3:c.7320G>C
|
XP_006724537.1:p.Gln2440His
|
|
XM_011545468.2:c.7320G>C
|
XP_011543770.1:p.Gln2440His
|
|
XM_017029328.1:c.7320G>C
|
XP_016884817.1:p.Gln2440His
|
|
XM_017029331.1:c.1494G>C
|
XP_016884820.1:p.Gln498His
|
|
NM_000109.4:c.7296G>C
|
NP_000100.3:p.Gln2432His
|
|
NM_004006.3:c.7320G>C
MANE Select
|
NP_003997.2:p.Gln2440His
|
|
NM_004011.4:c.3297G>C
|
NP_004002.3:p.Gln1099His
|
|
NM_004012.4:c.3288G>C
|
NP_004003.2:p.Gln1096His
|
|
NM_004021.3:c.-61G>C
|
NP_004012.2:n.-61G>C
|
|
NM_004023.3:c.-61G>C
|
NP_004014.2:n.-61G>C
|
|
NM_004013.3:c.-61G>C
|
NP_004004.2:n.-61G>C
|
|
NM_004020.4:c.-61G>C
|
NP_004011.3:n.-61G>C
|
|
NM_004022.3:c.-61G>C
|
NP_004013.2:n.-61G>C
|
|