|
ENST00000219548.9:c.423_424delinsCG
(STUB1)
MANE Select
|
ENSP00000219548.4:p.Ile141=
|
|
|
ENST00000219548.8:c.423_424delinsCG
(STUB1)
|
ENSP00000219548.4:p.Ile141=
|
|
|
ENST00000563505.5:n.519_520delinsCG
(STUB1)
|
|
|
|
ENST00000564316.1:c.22_23delinsCG
(STUB1)
|
|
|
|
ENST00000564370.5:c.207_208delinsCG
(STUB1)
|
ENSP00000456875.1:p.Ile69=
|
|
|
ENST00000565677.5:c.207_208delinsCG
(STUB1)
|
ENSP00000457228.1:p.Ile69=
|
|
|
ENST00000566181.2:n.192_193delinsCG
(STUB1)
|
|
|
|
ENST00000566408.5:c.140_141delinsCG
(STUB1)
|
|
|
|
ENST00000567173.5:c.366_367delinsCG
(STUB1)
|
ENSP00000456591.1:p.Ile122=
|
|
|
ENST00000569248.5:n.997_998delinsCG
(STUB1)
|
|
|
|
ENST00000620831.4:c.-50+38199_-50+38200delinsCG
(MSLN)
|
ENSP00000482893.1:n.-50+38199_-50+38200delinsCG
|
|
|
NM_001293197.1:c.207_208delinsCG
(STUB1)
|
NP_001280126.1:p.Ile69=
|
|
|
NM_005861.3:c.423_424delinsCG
(STUB1)
|
NP_005852.2:p.Ile141=
|
|
|
NM_005861.4:c.423_424delinsCG
(STUB1)
MANE Select
|
NP_005852.2:p.Ile141=
|
|
|
NM_001293197.2:c.207_208delinsCG
(STUB1)
|
NP_001280126.1:p.Ile69=
|
|
