ENST00000461073.6:c.*2499G>C
|
ENSP00000419905.1:n.*2499G>C
|
|
ENST00000483553.6:c.*512G>C
|
ENSP00000420332.2:n.*512G>C
|
|
ENST00000485349.6:n.4016+5G>C
|
|
|
ENST00000491994.2:c.3545G>C
|
ENSP00000417586.2:p.Ser1182Thr
|
|
ENST00000494058.6:n.3842+5G>C
|
|
|
ENST00000697831.1:c.3471+5G>C
|
ENSP00000513453.1:n.3471+5G>C
|
|
ENST00000697832.1:n.3693+5G>C
|
|
|
ENST00000697833.1:c.*488+5G>C
|
ENSP00000513454.1:n.*488+5G>C
|
|
ENST00000697834.1:n.4169G>C
|
|
|
ENST00000697835.1:c.*3058+5G>C
|
ENSP00000513455.1:n.*3058+5G>C
|
|
ENST00000697836.1:n.3871+5G>C
|
|
|
ENST00000697837.1:c.*656+5G>C
|
ENSP00000513456.1:n.*656+5G>C
|
|
ENST00000697838.1:c.3405+5G>C
|
ENSP00000513457.1:n.3405+5G>C
|
|
ENST00000697839.1:n.4263G>C
|
|
|
ENST00000697840.1:c.3576+5G>C
|
ENSP00000513458.1:n.3576+5G>C
|
|
ENST00000697841.1:n.4362G>C
|
|
|
ENST00000697842.1:n.3795+5G>C
|
|
|
ENST00000375394.7:c.3540+5G>C
MANE Select
|
ENSP00000364543.2:n.3540+5G>C
|
|
ENST00000375394.6:c.3540+5G>C
|
ENSP00000364543.2:n.3540+5G>C
|
|
ENST00000465703.5:n.4181G>C
|
|
|
ENST00000470453.1:n.383-90G>C
|
|
|
ENST00000471818.1:n.469+5G>C
|
|
|
ENST00000474839.5:c.*2912+5G>C
|
ENSP00000420470.1:n.*2912+5G>C
|
|
ENST00000483553.5:c.981G>C
|
|
|
ENST00000491994.1:c.540G>C
|
|
|
NM_006929.4:c.3540+5G>C
|
NP_008860.4:n.3540+5G>C
|
|
XR_001743586.2:n.3644G>C
|
|
|
XR_926301.3:n.3556+5G>C
|
|
|
NM_006929.5:c.3540+5G>C
MANE Select
|
NP_008860.4:n.3540+5G>C
|
|