ENST00000368485.8:c.1228T>A
MANE Select
|
ENSP00000357470.3:p.Leu410Met
|
|
ENST00000344086.8:c.*36T>A
|
ENSP00000340589.4:n.*36T>A
|
|
ENST00000368485.7:c.1228T>A
|
ENSP00000357470.3:p.Leu410Met
|
|
ENST00000502679.1:n.541T>A
|
|
|
ENST00000507256.1:n.426T>A
|
|
|
NM_000565.3:c.1228T>A
|
NP_000556.1:p.Leu410Met
|
|
NM_181359.2:c.*36T>A
|
NP_852004.1:n.*36T>A
|
|
XM_005245139.1:c.992T>A
|
XP_005245196.1:p.Phe331Tyr
|
|
XM_005245140.1:c.*69T>A
|
XP_005245197.1:n.*69T>A
|
|
XM_006711298.1:c.1276T>A
|
XP_006711361.1:p.Leu426Met
|
|
XM_006711299.2:c.*36T>A
|
XP_006711362.1:n.*36T>A
|
|
XM_005245139.2:c.992T>A
|
XP_005245196.1:p.Phe331Tyr
|
|
XM_005245140.3:c.*69T>A
|
XP_005245197.1:n.*69T>A
|
|
XM_006711298.2:c.1276T>A
|
XP_006711361.1:p.Leu426Met
|
|
XM_006711299.4:c.*36T>A
|
XP_006711362.1:n.*36T>A
|
|
XM_017001199.2:c.1375T>A
|
XP_016856688.1:p.Leu459Met
|
|
XM_017001200.2:c.1327T>A
|
XP_016856689.1:p.Leu443Met
|
|
XM_017001201.2:c.*69T>A
|
XP_016856690.1:n.*69T>A
|
|
NM_000565.4:c.1228T>A
MANE Select
|
NP_000556.1:p.Leu410Met
|
|
NM_181359.3:c.*36T>A
|
NP_852004.1:n.*36T>A
|
|
NM_001382769.1:c.1327T>A
|
NP_001369698.1:p.Leu443Met
|
|
NM_001382770.1:c.1321T>A
|
NP_001369699.1:p.Leu441Met
|
|
NM_001382771.1:c.1276T>A
|
NP_001369700.1:p.Leu426Met
|
|
NM_001382772.1:c.1222T>A
|
NP_001369701.1:p.Leu408Met
|
|
NM_001382773.1:c.*36T>A
|
NP_001369702.1:n.*36T>A
|
|
NM_001382774.1:c.868T>A
|
NP_001369703.1:p.Leu290Met
|
|