ENST00000361669.7:c.2391+5092T>A
MANE Select
|
ENSP00000355316.2:n.2391+5092T>A
|
|
ENST00000361669.6:c.2391+5092T>A
|
ENSP00000355316.2:n.2391+5092T>A
|
|
ENST00000439827.1:c.1325-5373T>A
|
ENSP00000398767.1:n.1325-5373T>A
|
|
NM_000840.2:c.2391+5092T>A
|
NP_000831.2:n.2391+5092T>A
|
|
XM_011516088.1:c.1325-5373T>A
|
XP_011514390.1:n.1325-5373T>A
|
|
NM_001363522.1:c.1325-5373T>A
|
NP_001350451.1:n.1325-5373T>A
|
|
NM_000840.3:c.2391+5092T>A
MANE Select
|
NP_000831.2:n.2391+5092T>A
|
|
NM_001363522.2:c.1325-5373T>A
|
NP_001350451.1:n.1325-5373T>A
|
|