ENST00000232607.7:c.538C>G
MANE Select
|
ENSP00000232607.2:p.Leu180Val
|
|
ENST00000232607.6:c.538C>G
|
ENSP00000232607.2:p.Leu180Val
|
|
ENST00000460034.5:c.*282C>G
|
ENSP00000420409.1:n.*282C>G
|
|
ENST00000462091.5:c.*210C>G
|
ENSP00000417893.1:n.*210C>G
|
|
ENST00000467167.5:c.*436C>G
|
ENSP00000419618.1:n.*436C>G
|
|
ENST00000474588.5:c.311-120C>G
|
ENSP00000420348.1:n.311-120C>G
|
|
ENST00000479719.5:c.538C>G
|
ENSP00000420754.1:p.Leu180Val
|
|
ENST00000497791.5:c.*210C>G
|
ENSP00000419121.1:n.*210C>G
|
|
ENST00000498715.1:n.256C>G
|
|
|
NM_000373.3:c.538C>G
|
NP_000364.1:p.Leu180Val
|
|
NR_033434.1:n.490C>G
|
|
|
NR_033437.1:n.743C>G
|
|
|
XR_001740253.2:n.568C>G
|
|
|
NM_000373.4:c.538C>G
MANE Select
|
NP_000364.1:p.Leu180Val
|
|
NR_033434.2:n.404C>G
|
|
|
NR_033437.2:n.657C>G
|
|
|