|
NM_004984.4:c.2300+7G>A
MANE Select
|
NP_004975.2:n.2300+7G>A
|
|
ENST00000455537.7:c.2300+7G>A
MANE Select
|
ENSP00000408979.2:n.2300+7G>A
|
|
NM_001354705.1:c.2033+7G>A
|
NP_001341634.1:n.2033+7G>A
|
|
NM_001354705.2:c.2033+7G>A
|
NP_001341634.1:n.2033+7G>A
|
|
NM_004984.2:c.2300+7G>A
|
NP_004975.2:n.2300+7G>A
|
|
NM_004984.3:c.2300+7G>A
|
NP_004975.2:n.2300+7G>A
|
|
ENST00000286452.5:c.2033+7G>A
|
ENSP00000286452.5:n.2033+7G>A
|
|
ENST00000455537.6:c.2300+7G>A
|
ENSP00000408979.2:n.2300+7G>A
|
|
ENST00000674619.1:c.2300+7G>A
|
ENSP00000502270.1:n.2300+7G>A
|
|
ENST00000675397.1:n.70+7G>A
|
|
|
ENST00000675882.1:n.1287+7G>A
|
|
|
ENST00000675929.1:n.858+7G>A
|
|
|
ENST00000675984.1:n.2370+7G>A
|
|
|
ENST00000676081.1:n.1945+7G>A
|
|
|
ENST00000676457.1:c.2195+7G>A
|
ENSP00000501588.1:n.2195+7G>A
|
|
XR_002957324.1:n.2533+7G>A
|
|