ENST00000265517.10:c.2639T>A
MANE Select
|
ENSP00000265517.5:p.Val880Glu
|
|
ENST00000457717.6:c.2639T>A
|
ENSP00000400821.1:p.Val880Glu
|
|
ENST00000511045.6:c.2390T>A
|
ENSP00000427679.2:p.Val797Glu
|
|
ENST00000265517.9:c.2639T>A
|
ENSP00000265517.5:p.Val880Glu
|
|
ENST00000457717.5:c.2639T>A
|
ENSP00000400821.1:p.Val880Glu
|
|
ENST00000511045.5:c.2720T>A
|
ENSP00000427679.1:p.Val907Glu
|
|
ENST00000619629.1:c.*1086T>A
|
ENSP00000482850.1:n.*1086T>A
|
|
NM_000253.3:c.2639T>A
|
NP_000244.2:p.Val880Glu
|
|
NM_001300785.1:c.2720T>A
|
NP_001287714.1:p.Val907Glu
|
|
NM_000253.4:c.2639T>A
|
NP_000244.2:p.Val880Glu
|
|
NM_001300785.2:c.2390T>A
|
NP_001287714.2:p.Val797Glu
|
|
NM_001386140.1:c.2639T>A
MANE Select
|
NP_001373069.1:p.Val880Glu
|
|