ENST00000461073.6:c.*2501A>T
|
ENSP00000419905.1:n.*2501A>T
|
|
ENST00000483553.6:c.*514A>T
|
ENSP00000420332.2:n.*514A>T
|
|
ENST00000485349.6:n.4016+7A>T
|
|
|
ENST00000491994.2:c.3547A>T
|
ENSP00000417586.2:p.Thr1183Ser
|
|
ENST00000494058.6:n.3842+7A>T
|
|
|
ENST00000697831.1:c.3471+7A>T
|
ENSP00000513453.1:n.3471+7A>T
|
|
ENST00000697832.1:n.3693+7A>T
|
|
|
ENST00000697833.1:c.*488+7A>T
|
ENSP00000513454.1:n.*488+7A>T
|
|
ENST00000697834.1:n.4171A>T
|
|
|
ENST00000697835.1:c.*3058+7A>T
|
ENSP00000513455.1:n.*3058+7A>T
|
|
ENST00000697836.1:n.3871+7A>T
|
|
|
ENST00000697837.1:c.*656+7A>T
|
ENSP00000513456.1:n.*656+7A>T
|
|
ENST00000697838.1:c.3405+7A>T
|
ENSP00000513457.1:n.3405+7A>T
|
|
ENST00000697839.1:n.4265A>T
|
|
|
ENST00000697840.1:c.3576+7A>T
|
ENSP00000513458.1:n.3576+7A>T
|
|
ENST00000697841.1:n.4364A>T
|
|
|
ENST00000697842.1:n.3795+7A>T
|
|
|
ENST00000375394.7:c.3540+7A>T
MANE Select
|
ENSP00000364543.2:n.3540+7A>T
|
|
ENST00000375394.6:c.3540+7A>T
|
ENSP00000364543.2:n.3540+7A>T
|
|
ENST00000465703.5:n.4183A>T
|
|
|
ENST00000470453.1:n.383-88A>T
|
|
|
ENST00000471818.1:n.469+7A>T
|
|
|
ENST00000474839.5:c.*2912+7A>T
|
ENSP00000420470.1:n.*2912+7A>T
|
|
ENST00000483553.5:c.983A>T
|
|
|
ENST00000491994.1:c.542A>T
|
|
|
NM_006929.4:c.3540+7A>T
|
NP_008860.4:n.3540+7A>T
|
|
XR_001743586.2:n.3646A>T
|
|
|
XR_926301.3:n.3556+7A>T
|
|
|
NM_006929.5:c.3540+7A>T
MANE Select
|
NP_008860.4:n.3540+7A>T
|
|