ENST00000360822.8:c.3488-7C>A
|
ENSP00000354065.4:n.3488-7C>A
|
|
ENST00000416449.6:c.4082-7C>A
|
ENSP00000400395.2:n.4082-7C>A
|
|
ENST00000479584.2:n.2425-7C>A
|
|
|
ENST00000684780.1:n.4468-7C>A
|
|
|
ENST00000685866.1:c.*2005-7C>A
|
ENSP00000509484.1:n.*2005-7C>A
|
|
ENST00000686376.1:c.4258-7C>A
|
ENSP00000510021.1:n.4258-7C>A
|
|
ENST00000686842.1:n.7732-7C>A
|
|
|
ENST00000687279.1:c.4175-7C>A
|
ENSP00000508692.1:n.4175-7C>A
|
|
ENST00000687311.1:n.4141-7C>A
|
|
|
ENST00000687633.1:c.4079-7C>A
|
ENSP00000510289.1:n.4079-7C>A
|
|
ENST00000688923.1:n.3550-7C>A
|
|
|
ENST00000689688.1:c.4178-7C>A
|
ENSP00000510155.1:n.4178-7C>A
|
|
ENST00000690646.1:c.4082-7C>A
|
ENSP00000510383.1:n.4082-7C>A
|
|
ENST00000690814.1:c.*1354-7C>A
|
ENSP00000508792.1:n.*1354-7C>A
|
|
ENST00000691504.1:n.4072-7C>A
|
|
|
ENST00000691551.1:c.347-7C>A
|
|
|
ENST00000692155.1:c.4258-7C>A
|
ENSP00000510290.1:n.4258-7C>A
|
|
ENST00000692746.1:n.4085-7C>A
|
|
|
ENST00000693386.1:c.4023-7C>A
|
ENSP00000510003.1:n.4023-7C>A
|
|
ENST00000693433.1:n.4072-7C>A
|
|
|
ENST00000693714.1:n.4125-7C>A
|
|
|
ENST00000693728.1:c.4082-7C>A
|
ENSP00000510580.1:n.4082-7C>A
|
|
ENST00000349780.9:c.4178-7C>A
MANE Select
|
ENSP00000343818.4:n.4178-7C>A
|
|
ENST00000349780.8:c.4178-7C>A
|
ENSP00000343818.4:n.4178-7C>A
|
|
ENST00000360190.8:c.4178-7C>A
|
ENSP00000353317.4:n.4178-7C>A
|
|
ENST00000360822.7:c.3488-7C>A
|
ENSP00000354065.4:n.3488-7C>A
|
|
ENST00000416449.5:c.2360-7C>A
|
ENSP00000400395.1:n.2360-7C>A
|
|
ENST00000425647.1:c.1208-7C>A
|
ENSP00000409941.1:n.1208-7C>A
|
|
ENST00000473282.6:c.*3002-7C>A
|
ENSP00000419265.1:n.*3002-7C>A
|
|
ENST00000480112.5:c.*2005-7C>A
|
ENSP00000418418.1:n.*2005-7C>A
|
|
ENST00000483412.5:n.3486-7C>A
|
|
|
NM_001011649.2:c.4178-7C>A
|
NP_001011649.1:n.4178-7C>A
|
|
NM_001272039.1:c.3488-7C>A
|
NP_001258968.1:n.3488-7C>A
|
|
NM_018249.5:c.4178-7C>A
|
NP_060719.4:n.4178-7C>A
|
|
NR_073554.1:n.4447-7C>A
|
|
|
NR_073555.1:n.4370-7C>A
|
|
|
NR_073556.1:n.4577-7C>A
|
|
|
NR_073557.1:n.4450-7C>A
|
|
|
NR_073558.1:n.4447-7C>A
|
|
|
XM_006717182.1:c.4082-7C>A
|
XP_006717245.1:n.4082-7C>A
|
|
XM_006717185.1:c.3491-7C>A
|
XP_006717248.1:n.3491-7C>A
|
|
XM_011518860.1:c.4175-7C>A
|
XP_011517162.1:n.4175-7C>A
|
|
XM_011518861.1:c.4175-7C>A
|
XP_011517163.1:n.4175-7C>A
|
|
XM_017014921.1:c.4079-7C>A
|
XP_016870410.1:n.4079-7C>A
|
|
XM_017014922.1:c.3344-7C>A
|
XP_016870411.1:n.3344-7C>A
|
|
XM_017014923.1:c.3491-7C>A
|
XP_016870412.1:n.3491-7C>A
|
|
XM_017014924.1:c.1973-7C>A
|
XP_016870413.1:n.1973-7C>A
|
|
NM_018249.6:c.4178-7C>A
MANE Select
|
NP_060719.4:n.4178-7C>A
|
|
NM_001011649.3:c.4178-7C>A
|
NP_001011649.1:n.4178-7C>A
|
|
NR_073554.2:n.4444-7C>A
|
|
|
NR_073555.2:n.4367-7C>A
|
|
|
NR_073556.2:n.4574-7C>A
|
|
|
NR_073557.2:n.4447-7C>A
|
|
|
NR_073558.2:n.4444-7C>A
|
|
|
NM_001272039.2:c.3488-7C>A
|
NP_001258968.1:n.3488-7C>A
|
|