|
ENST00000706954.1:c.-17+805G>A
(PTEN)
|
ENSP00000516674.1:n.-17+805G>A
|
|
|
ENST00000688308.1:c.-17+334G>A
(PTEN)
|
ENSP00000508752.1:n.-17+334G>A
|
|
|
ENST00000693560.1:c.-503G>A
(PTEN)
|
ENSP00000509861.1:n.-503G>A
|
|
|
ENST00000445946.5:c.-960C>T
(KLLN)
MANE Select
|
ENSP00000392204.2:n.-960C>T
|
|
|
ENST00000371953.7:c.-1023G>A
(PTEN)
|
ENSP00000361021.3:n.-1023G>A
|
|
|
ENST00000610634.1:c.-1125G>A
(PTEN)
|
ENSP00000477517.1:n.-1125G>A
|
|
|
NM_000314.5:c.-1022G>A
(PTEN)
|
NP_000305.3:n.-1022G>A
|
|
|
NM_000314.6:c.-1022G>A
(PTEN)
|
NP_000305.3:n.-1022G>A
|
|
|
NM_001304717.2:c.-503G>A
(PTEN)
|
NP_001291646.2:n.-503G>A
|
|
|
NM_001304718.1:c.-1727G>A
(PTEN)
|
NP_001291647.1:n.-1727G>A
|
|
|
NM_001126049.2:c.-960C>T
(KLLN)
MANE Select
|
NP_001119521.1:n.-960C>T
|
|
