ENST00000461073.6:c.*2440G>T
|
ENSP00000419905.1:n.*2440G>T
|
|
ENST00000483553.6:c.*453G>T
|
ENSP00000420332.2:n.*453G>T
|
|
ENST00000485349.6:n.3962G>T
|
|
|
ENST00000491994.2:c.3486G>T
|
ENSP00000417586.2:p.Val1162=
|
|
ENST00000494058.6:n.3788G>T
|
|
|
ENST00000697831.1:c.3417G>T
|
ENSP00000513453.1:p.Val1139=
|
|
ENST00000697832.1:n.3639G>T
|
|
|
ENST00000697833.1:c.*434G>T
|
ENSP00000513454.1:n.*434G>T
|
|
ENST00000697834.1:n.4110G>T
|
|
|
ENST00000697835.1:c.*3004G>T
|
ENSP00000513455.1:n.*3004G>T
|
|
ENST00000697836.1:n.3817G>T
|
|
|
ENST00000697837.1:c.*602G>T
|
ENSP00000513456.1:n.*602G>T
|
|
ENST00000697838.1:c.3351G>T
|
ENSP00000513457.1:p.Val1117=
|
|
ENST00000697839.1:n.4204G>T
|
|
|
ENST00000697840.1:c.3522G>T
|
ENSP00000513458.1:p.Val1174=
|
|
ENST00000697841.1:n.4303G>T
|
|
|
ENST00000697842.1:n.3741G>T
|
|
|
ENST00000375394.7:c.3486G>T
MANE Select
|
ENSP00000364543.2:p.Val1162=
|
|
ENST00000375394.6:c.3486G>T
|
ENSP00000364543.2:p.Val1162=
|
|
ENST00000465703.5:n.4122G>T
|
|
|
ENST00000470453.1:n.382+50G>T
|
|
|
ENST00000471818.1:n.415G>T
|
|
|
ENST00000474839.5:c.*2858G>T
|
ENSP00000420470.1:n.*2858G>T
|
|
ENST00000483553.5:c.922G>T
|
|
|
ENST00000485349.5:n.692G>T
|
|
|
ENST00000491994.1:c.481G>T
|
|
|
NM_006929.4:c.3486G>T
|
NP_008860.4:p.Val1162=
|
|
XR_001743586.2:n.3585G>T
|
|
|
XR_926301.3:n.3502G>T
|
|
|
NM_006929.5:c.3486G>T
MANE Select
|
NP_008860.4:p.Val1162=
|
|