ENST00000684294.1:c.*749A>T
(NPHP3)
|
ENSP00000508078.1:n.*749A>T
|
|
ENST00000337331.10:c.2841A>T
(NPHP3)
MANE Select
|
ENSP00000338766.5:p.Glu947Asp
|
|
ENST00000337331.9:c.2841A>T
(NPHP3)
|
ENSP00000338766.5:p.Glu947Asp
|
|
ENST00000465756.5:c.*749A>T
(NPHP3)
|
ENSP00000419907.1:n.*749A>T
|
|
ENST00000471702.2:c.*832A>T
(NPHP3-ACAD11)
|
ENSP00000419763.1:n.*832A>T
|
|
ENST00000474871.5:n.575A>T
(NPHP3)
|
|
|
ENST00000490993.5:n.3566A>T
(NPHP3)
|
|
|
NM_153240.4:c.2841A>T
(NPHP3)
|
NP_694972.3:p.Glu947Asp
|
|
NR_037804.1:n.2847A>T
(NPHP3-ACAD11)
|
|
|
NM_153240.5:c.2841A>T
(NPHP3)
MANE Select
|
NP_694972.3:p.Glu947Asp
|
|