|
ENST00000706954.1:c.-17+809G>A
(PTEN)
|
ENSP00000516674.1:n.-17+809G>A
|
|
|
ENST00000688308.1:c.-17+338G>A
(PTEN)
|
ENSP00000508752.1:n.-17+338G>A
|
|
|
ENST00000693560.1:c.-499G>A
(PTEN)
|
ENSP00000509861.1:n.-499G>A
|
|
|
ENST00000445946.5:c.-964C>T
(KLLN)
MANE Select
|
ENSP00000392204.2:n.-964C>T
|
|
|
ENST00000371953.7:c.-1019G>A
(PTEN)
|
ENSP00000361021.3:n.-1019G>A
|
|
|
ENST00000610634.1:c.-1121G>A
(PTEN)
|
ENSP00000477517.1:n.-1121G>A
|
|
|
NM_000314.5:c.-1018G>A
(PTEN)
|
NP_000305.3:n.-1018G>A
|
|
|
NM_000314.6:c.-1018G>A
(PTEN)
|
NP_000305.3:n.-1018G>A
|
|
|
NM_001304717.2:c.-499G>A
(PTEN)
|
NP_001291646.2:n.-499G>A
|
|
|
NM_001304718.1:c.-1723G>A
(PTEN)
|
NP_001291647.1:n.-1723G>A
|
|
|
NM_001126049.2:c.-964C>T
(KLLN)
MANE Select
|
NP_001119521.1:n.-964C>T
|
|
