|
ENST00000706954.1:c.-17+835G>T
(PTEN)
|
ENSP00000516674.1:n.-17+835G>T
|
|
|
ENST00000688308.1:c.-17+364G>T
(PTEN)
|
ENSP00000508752.1:n.-17+364G>T
|
|
|
ENST00000693560.1:c.-473G>T
(PTEN)
|
ENSP00000509861.1:n.-473G>T
|
|
|
ENST00000445946.5:c.-990C>A
(KLLN)
MANE Select
|
ENSP00000392204.2:n.-990C>A
|
|
|
ENST00000371953.7:c.-993G>T
(PTEN)
|
ENSP00000361021.3:n.-993G>T
|
|
|
ENST00000610634.1:c.-1095G>T
(PTEN)
|
ENSP00000477517.1:n.-1095G>T
|
|
|
NM_000314.5:c.-992G>T
(PTEN)
|
NP_000305.3:n.-992G>T
|
|
|
NM_000314.6:c.-992G>T
(PTEN)
|
NP_000305.3:n.-992G>T
|
|
|
NM_001304717.2:c.-473G>T
(PTEN)
|
NP_001291646.2:n.-473G>T
|
|
|
NM_001304718.1:c.-1697G>T
(PTEN)
|
NP_001291647.1:n.-1697G>T
|
|
|
NM_001126049.2:c.-990C>A
(KLLN)
MANE Select
|
NP_001119521.1:n.-990C>A
|
|
