|
ENST00000700029.2:c.-845G>T
(PTEN)
|
ENSP00000514759.2:n.-845G>T
|
|
|
ENST00000710265.1:c.-845G>T
(PTEN)
|
ENSP00000518161.1:n.-845G>T
|
|
|
ENST00000706954.1:c.-16-829G>T
(PTEN)
|
ENSP00000516674.1:n.-16-829G>T
|
|
|
ENST00000706955.1:c.-845G>T
(PTEN)
|
ENSP00000516675.1:n.-845G>T
|
|
|
ENST00000688158.1:c.-845G>T
(PTEN)
|
ENSP00000509254.1:n.-845G>T
|
|
|
ENST00000688308.1:c.-17+512G>T
(PTEN)
|
ENSP00000508752.1:n.-17+512G>T
|
|
|
ENST00000692337.1:c.67G>T
(MLDHR)
|
ENSP00000509326.1:p.Val23Phe
|
|
|
ENST00000693560.1:c.-325G>T
(PTEN)
|
ENSP00000509861.1:n.-325G>T
|
|
|
ENST00000371953.8:c.-845G>T
(PTEN)
MANE Select
|
ENSP00000361021.3:n.-845G>T
|
|
|
ENST00000371953.7:c.-845G>T
(PTEN)
|
ENSP00000361021.3:n.-845G>T
|
|
|
ENST00000610634.1:c.-947G>T
(PTEN)
|
ENSP00000477517.1:n.-947G>T
|
|
|
NM_000314.5:c.-844G>T
(PTEN)
|
NP_000305.3:n.-844G>T
|
|
|
NM_000314.6:c.-844G>T
(PTEN)
|
NP_000305.3:n.-844G>T
|
|
|
NM_001304717.2:c.-325G>T
(PTEN)
|
NP_001291646.2:n.-325G>T
|
|
|
NM_001304718.1:c.-1549G>T
(PTEN)
|
NP_001291647.1:n.-1549G>T
|
|
|
NM_000314.7:c.-844G>T
(PTEN)
|
NP_000305.3:n.-844G>T
|
|
|
NM_001304717.5:c.-325G>T
(PTEN)
|
NP_001291646.4:n.-325G>T
|
|
|
NM_001304718.2:c.-1549G>T
(PTEN)
|
NP_001291647.1:n.-1549G>T
|
|
|
NM_000314.8:c.-845G>T
(PTEN)
MANE Select
|
NP_000305.3:n.-845G>T
|
|
