ENST00000455537.7:c.2945C>A
MANE Select
|
ENSP00000408979.2:p.Ser982Tyr
|
|
ENST00000674619.1:c.2966C>A
|
ENSP00000502270.1:p.Ser989Tyr
|
|
ENST00000675697.1:c.36C>A
|
|
|
ENST00000675737.1:n.349C>A
|
|
|
ENST00000675882.1:n.2468C>A
|
|
|
ENST00000675929.1:n.1503C>A
|
|
|
ENST00000676055.1:c.36C>A
|
|
|
ENST00000676457.1:c.2840C>A
|
ENSP00000501588.1:p.Ser947Tyr
|
|
ENST00000286452.5:c.2678C>A
|
ENSP00000286452.5:p.Ser893Tyr
|
|
ENST00000455537.6:c.2945C>A
|
ENSP00000408979.2:p.Ser982Tyr
|
|
ENST00000552227.1:n.228C>A
|
|
|
NM_004984.2:c.2945C>A
|
NP_004975.2:p.Ser982Tyr
|
|
NM_001354705.1:c.2678C>A
|
NP_001341634.1:p.Ser893Tyr
|
|
NM_004984.3:c.2945C>A
|
NP_004975.2:p.Ser982Tyr
|
|
XR_002957324.1:n.3178C>A
|
|
|
NM_004984.4:c.2945C>A
MANE Select
|
NP_004975.2:p.Ser982Tyr
|
|
NM_001354705.2:c.2678C>A
|
NP_001341634.1:p.Ser893Tyr
|
|