ENST00000461073.6:c.*2423A>T
|
ENSP00000419905.1:n.*2423A>T
|
|
ENST00000483553.6:c.*436A>T
|
ENSP00000420332.2:n.*436A>T
|
|
ENST00000485349.6:n.3945A>T
|
|
|
ENST00000491994.2:c.3469A>T
|
ENSP00000417586.2:p.Thr1157Ser
|
|
ENST00000494058.6:n.3771A>T
|
|
|
ENST00000697831.1:c.3400A>T
|
ENSP00000513453.1:p.Thr1134Ser
|
|
ENST00000697832.1:n.3622A>T
|
|
|
ENST00000697833.1:c.*417A>T
|
ENSP00000513454.1:n.*417A>T
|
|
ENST00000697834.1:n.4093A>T
|
|
|
ENST00000697835.1:c.*2987A>T
|
ENSP00000513455.1:n.*2987A>T
|
|
ENST00000697836.1:n.3800A>T
|
|
|
ENST00000697837.1:c.*585A>T
|
ENSP00000513456.1:n.*585A>T
|
|
ENST00000697838.1:c.3334A>T
|
ENSP00000513457.1:p.Thr1112Ser
|
|
ENST00000697839.1:n.4187A>T
|
|
|
ENST00000697840.1:c.3505A>T
|
ENSP00000513458.1:p.Thr1169Ser
|
|
ENST00000697841.1:n.4286A>T
|
|
|
ENST00000697842.1:n.3724A>T
|
|
|
ENST00000375394.7:c.3469A>T
MANE Select
|
ENSP00000364543.2:p.Thr1157Ser
|
|
ENST00000375394.6:c.3469A>T
|
ENSP00000364543.2:p.Thr1157Ser
|
|
ENST00000465703.5:n.4105A>T
|
|
|
ENST00000470453.1:n.382+33A>T
|
|
|
ENST00000471818.1:n.398A>T
|
|
|
ENST00000474839.5:c.*2841A>T
|
ENSP00000420470.1:n.*2841A>T
|
|
ENST00000483553.5:c.905A>T
|
|
|
ENST00000485349.5:n.675A>T
|
|
|
ENST00000491994.1:c.464A>T
|
|
|
NM_006929.4:c.3469A>T
|
NP_008860.4:p.Thr1157Ser
|
|
XR_001743586.2:n.3568A>T
|
|
|
XR_926301.3:n.3485A>T
|
|
|
NM_006929.5:c.3469A>T
MANE Select
|
NP_008860.4:p.Thr1157Ser
|
|