ENST00000368485.8:c.1213C>G
MANE Select
|
ENSP00000357470.3:p.His405Asp
|
|
ENST00000344086.8:c.*21C>G
|
ENSP00000340589.4:n.*21C>G
|
|
ENST00000368485.7:c.1213C>G
|
ENSP00000357470.3:p.His405Asp
|
|
ENST00000502679.1:n.526C>G
|
|
|
ENST00000507256.1:n.411C>G
|
|
|
NM_000565.3:c.1213C>G
|
NP_000556.1:p.His405Asp
|
|
NM_181359.2:c.*21C>G
|
NP_852004.1:n.*21C>G
|
|
XM_005245139.1:c.977C>G
|
XP_005245196.1:p.Ala326Gly
|
|
XM_005245140.1:c.*54C>G
|
XP_005245197.1:n.*54C>G
|
|
XM_006711298.1:c.1261C>G
|
XP_006711361.1:p.His421Asp
|
|
XM_006711299.2:c.*21C>G
|
XP_006711362.1:n.*21C>G
|
|
XM_005245139.2:c.977C>G
|
XP_005245196.1:p.Ala326Gly
|
|
XM_005245140.3:c.*54C>G
|
XP_005245197.1:n.*54C>G
|
|
XM_006711298.2:c.1261C>G
|
XP_006711361.1:p.His421Asp
|
|
XM_006711299.4:c.*21C>G
|
XP_006711362.1:n.*21C>G
|
|
XM_017001199.2:c.1360C>G
|
XP_016856688.1:p.His454Asp
|
|
XM_017001200.2:c.1312C>G
|
XP_016856689.1:p.His438Asp
|
|
XM_017001201.2:c.*54C>G
|
XP_016856690.1:n.*54C>G
|
|
NM_000565.4:c.1213C>G
MANE Select
|
NP_000556.1:p.His405Asp
|
|
NM_181359.3:c.*21C>G
|
NP_852004.1:n.*21C>G
|
|
NM_001382769.1:c.1312C>G
|
NP_001369698.1:p.His438Asp
|
|
NM_001382770.1:c.1306C>G
|
NP_001369699.1:p.His436Asp
|
|
NM_001382771.1:c.1261C>G
|
NP_001369700.1:p.His421Asp
|
|
NM_001382772.1:c.1207C>G
|
NP_001369701.1:p.His403Asp
|
|
NM_001382773.1:c.*21C>G
|
NP_001369702.1:n.*21C>G
|
|
NM_001382774.1:c.853C>G
|
NP_001369703.1:p.His285Asp
|
|