ENST00000474627.8:c.732+88T>C
MANE Select
|
ENSP00000417190.2:n.732+88T>C
|
|
ENST00000462733.5:c.*149+88T>C
|
ENSP00000463920.1:n.*149+88T>C
|
|
ENST00000465337.2:n.592-37T>C
|
|
|
ENST00000467560.5:n.142+88T>C
|
|
|
ENST00000469327.5:n.642+88T>C
|
|
|
ENST00000474627.7:c.732+88T>C
|
ENSP00000417190.2:n.732+88T>C
|
|
ENST00000488753.1:n.528-37T>C
|
|
|
ENST00000496852.5:n.1237+88T>C
|
|
|
ENST00000581698.1:c.49-2349T>C
|
|
|
ENST00000584205.5:c.*33+3589T>C
|
ENSP00000462899.1:n.*33+3589T>C
|
|
ENST00000585101.5:c.*33+3589T>C
|
ENSP00000463861.1:n.*33+3589T>C
|
|
NM_145691.3:c.732+88T>C
|
NP_663729.1:n.732+88T>C
|
|
XM_005256848.2:c.733-37T>C
|
XP_005256905.1:n.733-37T>C
|
|
XM_011524062.1:c.732+88T>C
|
XP_011522364.1:n.732+88T>C
|
|
XM_011524063.1:c.732+88T>C
|
XP_011522365.1:n.732+88T>C
|
|
XM_011524064.1:c.432+88T>C
|
XP_011522366.1:n.432+88T>C
|
|
XM_011524065.1:c.732+88T>C
|
XP_011522367.1:n.732+88T>C
|
|
XM_011524066.1:c.195+88T>C
|
XP_011522368.1:n.195+88T>C
|
|
XM_005256848.4:c.733-37T>C
|
XP_005256905.1:n.733-37T>C
|
|
XM_011524065.2:c.732+88T>C
|
XP_011522367.1:n.732+88T>C
|
|
XM_017025302.1:c.432+88T>C
|
XP_016880791.1:n.432+88T>C
|
|
XM_017025303.1:c.432+88T>C
|
XP_016880792.1:n.432+88T>C
|
|
XR_001752677.2:n.1129+88T>C
|
|
|
NM_145691.4:c.732+88T>C
MANE Select
|
NP_663729.1:n.732+88T>C
|
|