ENST00000455537.7:c.2921C>G
MANE Select
|
ENSP00000408979.2:p.Ser974Cys
|
|
ENST00000674619.1:c.2942C>G
|
ENSP00000502270.1:p.Ser981Cys
|
|
ENST00000675697.1:c.12C>G
|
|
|
ENST00000675737.1:n.325C>G
|
|
|
ENST00000675882.1:n.2444C>G
|
|
|
ENST00000675929.1:n.1479C>G
|
|
|
ENST00000676055.1:c.12C>G
|
|
|
ENST00000676457.1:c.2816C>G
|
ENSP00000501588.1:p.Ser939Cys
|
|
ENST00000286452.5:c.2654C>G
|
ENSP00000286452.5:p.Ser885Cys
|
|
ENST00000455537.6:c.2921C>G
|
ENSP00000408979.2:p.Ser974Cys
|
|
ENST00000552227.1:n.204C>G
|
|
|
NM_004984.2:c.2921C>G
|
NP_004975.2:p.Ser974Cys
|
|
NM_001354705.1:c.2654C>G
|
NP_001341634.1:p.Ser885Cys
|
|
NM_004984.3:c.2921C>G
|
NP_004975.2:p.Ser974Cys
|
|
XR_002957324.1:n.3154C>G
|
|
|
NM_004984.4:c.2921C>G
MANE Select
|
NP_004975.2:p.Ser974Cys
|
|
NM_001354705.2:c.2654C>G
|
NP_001341634.1:p.Ser885Cys
|
|