ENST00000461073.6:c.*2410T>A
|
ENSP00000419905.1:n.*2410T>A
|
|
ENST00000483553.6:c.*423T>A
|
ENSP00000420332.2:n.*423T>A
|
|
ENST00000485349.6:n.3932T>A
|
|
|
ENST00000491994.2:c.3456T>A
|
ENSP00000417586.2:p.Cys1152Ter
|
|
ENST00000494058.6:n.3758T>A
|
|
|
ENST00000697831.1:c.3387T>A
|
ENSP00000513453.1:p.Cys1129Ter
|
|
ENST00000697832.1:n.3609T>A
|
|
|
ENST00000697833.1:c.*404T>A
|
ENSP00000513454.1:n.*404T>A
|
|
ENST00000697834.1:n.4080T>A
|
|
|
ENST00000697835.1:c.*2974T>A
|
ENSP00000513455.1:n.*2974T>A
|
|
ENST00000697836.1:n.3787T>A
|
|
|
ENST00000697837.1:c.*572T>A
|
ENSP00000513456.1:n.*572T>A
|
|
ENST00000697838.1:c.3321T>A
|
ENSP00000513457.1:p.Cys1107Ter
|
|
ENST00000697839.1:n.4174T>A
|
|
|
ENST00000697840.1:c.3492T>A
|
ENSP00000513458.1:p.Cys1164Ter
|
|
ENST00000697841.1:n.4273T>A
|
|
|
ENST00000697842.1:n.3711T>A
|
|
|
ENST00000375394.7:c.3456T>A
MANE Select
|
ENSP00000364543.2:p.Cys1152Ter
|
|
ENST00000375394.6:c.3456T>A
|
ENSP00000364543.2:p.Cys1152Ter
|
|
ENST00000465703.5:n.4092T>A
|
|
|
ENST00000470453.1:n.382+20T>A
|
|
|
ENST00000471818.1:n.385T>A
|
|
|
ENST00000474839.5:c.*2828T>A
|
ENSP00000420470.1:n.*2828T>A
|
|
ENST00000483553.5:c.892T>A
|
|
|
ENST00000485349.5:n.662T>A
|
|
|
ENST00000491994.1:c.451T>A
|
|
|
NM_006929.4:c.3456T>A
|
NP_008860.4:p.Cys1152Ter
|
|
XR_001743586.2:n.3555T>A
|
|
|
XR_926301.3:n.3472T>A
|
|
|
NM_006929.5:c.3456T>A
MANE Select
|
NP_008860.4:p.Cys1152Ter
|
|