ENST00000684294.1:c.*1277G>A
(NPHP3)
|
ENSP00000508078.1:n.*1277G>A
|
|
ENST00000337331.10:c.3369G>A
(NPHP3)
MANE Select
|
ENSP00000338766.5:p.Arg1123=
|
|
ENST00000337331.9:c.3369G>A
(NPHP3)
|
ENSP00000338766.5:p.Arg1123=
|
|
ENST00000465756.5:c.*1277G>A
(NPHP3)
|
ENSP00000419907.1:n.*1277G>A
|
|
ENST00000471702.2:c.*1360G>A
(NPHP3-ACAD11)
|
ENSP00000419763.1:n.*1360G>A
|
|
ENST00000474871.5:n.2568G>A
(NPHP3)
|
|
|
ENST00000490993.5:n.4094G>A
(NPHP3)
|
|
|
ENST00000493732.5:n.69G>A
(NPHP3)
|
|
|
ENST00000632629.1:c.16G>A
(NPHP3-ACAD11)
|
|
|
NM_153240.4:c.3369G>A
(NPHP3)
|
NP_694972.3:p.Arg1123=
|
|
NR_037804.1:n.3375G>A
(NPHP3-ACAD11)
|
|
|
NM_153240.5:c.3369G>A
(NPHP3)
MANE Select
|
NP_694972.3:p.Arg1123=
|
|