ENST00000461073.6:c.*2403T>A
|
ENSP00000419905.1:n.*2403T>A
|
|
ENST00000483553.6:c.*416T>A
|
ENSP00000420332.2:n.*416T>A
|
|
ENST00000485349.6:n.3925T>A
|
|
|
ENST00000491994.2:c.3449T>A
|
ENSP00000417586.2:p.Val1150Glu
|
|
ENST00000494058.6:n.3751T>A
|
|
|
ENST00000697831.1:c.3380T>A
|
ENSP00000513453.1:p.Val1127Glu
|
|
ENST00000697832.1:n.3602T>A
|
|
|
ENST00000697833.1:c.*397T>A
|
ENSP00000513454.1:n.*397T>A
|
|
ENST00000697834.1:n.4073T>A
|
|
|
ENST00000697835.1:c.*2967T>A
|
ENSP00000513455.1:n.*2967T>A
|
|
ENST00000697836.1:n.3780T>A
|
|
|
ENST00000697837.1:c.*565T>A
|
ENSP00000513456.1:n.*565T>A
|
|
ENST00000697838.1:c.3314T>A
|
ENSP00000513457.1:p.Val1105Glu
|
|
ENST00000697839.1:n.4167T>A
|
|
|
ENST00000697840.1:c.3485T>A
|
ENSP00000513458.1:p.Val1162Glu
|
|
ENST00000697841.1:n.4266T>A
|
|
|
ENST00000697842.1:n.3704T>A
|
|
|
ENST00000375394.7:c.3449T>A
MANE Select
|
ENSP00000364543.2:p.Val1150Glu
|
|
ENST00000375394.6:c.3449T>A
|
ENSP00000364543.2:p.Val1150Glu
|
|
ENST00000465703.5:n.4085T>A
|
|
|
ENST00000470453.1:n.382+13T>A
|
|
|
ENST00000471818.1:n.378T>A
|
|
|
ENST00000474839.5:c.*2821T>A
|
ENSP00000420470.1:n.*2821T>A
|
|
ENST00000483553.5:c.885T>A
|
|
|
ENST00000485349.5:n.655T>A
|
|
|
ENST00000491994.1:c.444T>A
|
|
|
NM_006929.4:c.3449T>A
|
NP_008860.4:p.Val1150Glu
|
|
XR_001743586.2:n.3548T>A
|
|
|
XR_926301.3:n.3465T>A
|
|
|
NM_006929.5:c.3449T>A
MANE Select
|
NP_008860.4:p.Val1150Glu
|
|