|
ENST00000706954.1:c.-17+837_-17+838delinsCT
(PTEN)
|
ENSP00000516674.1:n.-17+837_-17+838delinsCT
|
|
|
ENST00000688308.1:c.-17+366_-17+367delinsCT
(PTEN)
|
ENSP00000508752.1:n.-17+366_-17+367delinsCT
|
|
|
ENST00000693560.1:c.-471_-470delinsCT
(PTEN)
|
ENSP00000509861.1:n.-471_-470delinsCT
|
|
|
ENST00000445946.5:c.-993_-992delinsAG
(KLLN)
MANE Select
|
ENSP00000392204.2:n.-993_-992delinsAG
|
|
|
ENST00000371953.7:c.-991_-990delinsCT
(PTEN)
|
ENSP00000361021.3:n.-991_-990delinsCT
|
|
|
ENST00000610634.1:c.-1093_-1092delinsCT
(PTEN)
|
ENSP00000477517.1:n.-1093_-1092delinsCT
|
|
|
NM_000314.5:c.-990_-989delinsCT
(PTEN)
|
NP_000305.3:n.-990_-989delinsCT
|
|
|
NM_000314.6:c.-990_-989delinsCT
(PTEN)
|
NP_000305.3:n.-990_-989delinsCT
|
|
|
NM_001304717.2:c.-471_-470delinsCT
(PTEN)
|
NP_001291646.2:n.-471_-470delinsCT
|
|
|
NM_001304718.1:c.-1695_-1694delinsCT
(PTEN)
|
NP_001291647.1:n.-1695_-1694delinsCT
|
|
|
NM_001126049.2:c.-993_-992delinsAG
(KLLN)
MANE Select
|
NP_001119521.1:n.-993_-992delinsAG
|
|
