ENST00000362061.4:c.3791T>G
MANE Select
|
ENSP00000355192.3:p.Phe1264Cys
|
|
ENST00000679417.1:c.*2954T>G
|
ENSP00000506706.1:n.*2954T>G
|
|
ENST00000680051.1:n.917T>G
|
|
|
ENST00000680059.1:c.*1309T>G
|
ENSP00000504944.1:n.*1309T>G
|
|
ENST00000681078.1:c.3791T>G
|
ENSP00000506645.1:p.Phe1264Cys
|
|
ENST00000681190.1:c.3791T>G
|
ENSP00000506428.1:p.Phe1264Cys
|
|
ENST00000681874.1:c.3731T>G
|
ENSP00000505162.1:p.Phe1244Cys
|
|
ENST00000362061.3:c.3791T>G
|
ENSP00000355192.3:p.Phe1264Cys
|
|
ENST00000367338.7:c.3734T>G
|
ENSP00000356307.3:p.Phe1245Cys
|
|
NM_000069.2:c.3791T>G
|
NP_000060.2:p.Phe1264Cys
|
|
XM_005245478.2:c.3734T>G
|
XP_005245535.1:p.Phe1245Cys
|
|
XM_005245478.3:c.3734T>G
|
XP_005245535.1:p.Phe1245Cys
|
|
NM_000069.3:c.3791T>G
MANE Select
|
NP_000060.2:p.Phe1264Cys
|
|