ENST00000368507.8:c.6715+1667G>A
MANE Select
|
ENSP00000357493.3:n.6715+1667G>A
|
|
ENST00000368507.7:c.6715+1667G>A
|
ENSP00000357493.3:n.6715+1667G>A
|
|
ENST00000368508.7:c.6733+1667G>A
|
ENSP00000357494.3:n.6733+1667G>A
|
|
NM_002944.2:c.6733+1667G>A
|
NP_002935.2:n.6733+1667G>A
|
|
XM_006715548.2:c.6718+1667G>A
|
XP_006715611.1:n.6718+1667G>A
|
|
XM_011536049.1:c.6763+1667G>A
|
XP_011534351.1:n.6763+1667G>A
|
|
XM_011536050.1:c.6760+1667G>A
|
XP_011534352.1:n.6760+1667G>A
|
|
XM_011536051.1:c.6736+1667G>A
|
XP_011534353.1:n.6736+1667G>A
|
|
XM_011536052.1:c.6721+1667G>A
|
XP_011534354.1:n.6721+1667G>A
|
|
XM_011536053.1:c.6589+1667G>A
|
XP_011534355.1:n.6589+1667G>A
|
|
XM_011536054.1:c.6599+9487G>A
|
XP_011534356.1:n.6599+9487G>A
|
|
XM_006715548.4:c.6718+1667G>A
|
XP_006715611.1:n.6718+1667G>A
|
|
XM_011536049.2:c.6763+1667G>A
|
XP_011534351.1:n.6763+1667G>A
|
|
XM_011536050.2:c.6760+1667G>A
|
XP_011534352.1:n.6760+1667G>A
|
|
XM_011536051.2:c.6736+1667G>A
|
XP_011534353.1:n.6736+1667G>A
|
|
XM_011536052.2:c.6721+1667G>A
|
XP_011534354.1:n.6721+1667G>A
|
|
XM_011536053.2:c.6589+1667G>A
|
XP_011534355.1:n.6589+1667G>A
|
|
XM_011536054.2:c.6599+9487G>A
|
XP_011534356.1:n.6599+9487G>A
|
|
XM_017011172.1:c.6694+1667G>A
|
XP_016866661.1:n.6694+1667G>A
|
|
XM_017011173.1:c.6691+1667G>A
|
XP_016866662.1:n.6691+1667G>A
|
|
NM_001378891.1:c.6721+1667G>A
|
NP_001365820.1:n.6721+1667G>A
|
|
NM_001378902.1:c.6715+1667G>A
MANE Select
|
NP_001365831.1:n.6715+1667G>A
|
|
NM_002944.3:c.6733+1667G>A
|
NP_002935.2:n.6733+1667G>A
|
|