ENST00000496887.7:c.755T>G
|
ENSP00000434560.2:p.Phe252Cys
|
|
ENST00000646564.2:c.572T>G
|
ENSP00000495806.2:p.Phe191Cys
|
|
ENST00000155840.12:c.1016T>G
MANE Select
|
ENSP00000155840.2:p.Phe339Cys
|
|
ENST00000335475.6:c.635T>G
|
ENSP00000334497.5:p.Phe212Cys
|
|
ENST00000646564.1:c.218T>G
|
ENSP00000495806.1:p.Phe73Cys
|
|
ENST00000155840.9:c.1016T>G
|
ENSP00000155840.2:p.Phe339Cys
|
|
ENST00000335475.5:c.635T>G
|
ENSP00000334497.5:p.Phe212Cys
|
|
NM_000218.2:c.1016T>G , LRG_287t1:c.1016T>G
|
NP_000209.2:p.Phe339Cys
|
|
NM_181798.1:c.635T>G , LRG_287t2:c.635T>G
|
NP_861463.1:p.Phe212Cys
|
|
NM_000218.3:c.1016T>G
MANE Select
|
NP_000209.2:p.Phe339Cys
|
|