ENST00000455537.7:c.714+286A>C
MANE Select
|
ENSP00000408979.2:n.714+286A>C
|
|
ENST00000674619.1:c.714+286A>C
|
ENSP00000502270.1:n.714+286A>C
|
|
ENST00000676457.1:c.609+286A>C
|
ENSP00000501588.1:n.609+286A>C
|
|
ENST00000286452.5:c.447+286A>C
|
ENSP00000286452.5:n.447+286A>C
|
|
ENST00000455537.6:c.714+286A>C
|
ENSP00000408979.2:n.714+286A>C
|
|
NM_004984.2:c.714+286A>C
|
NP_004975.2:n.714+286A>C
|
|
NM_001354705.1:c.447+286A>C
|
NP_001341634.1:n.447+286A>C
|
|
NM_004984.3:c.714+286A>C
|
NP_004975.2:n.714+286A>C
|
|
XR_002957324.1:n.947+286A>C
|
|
|
NM_004984.4:c.714+286A>C
MANE Select
|
NP_004975.2:n.714+286A>C
|
|
NM_001354705.2:c.447+286A>C
|
NP_001341634.1:n.447+286A>C
|
|