ENST00000368485.8:c.1335C>G
MANE Select
|
ENSP00000357470.3:p.His445Gln
|
|
ENST00000344086.8:c.*143C>G
|
ENSP00000340589.4:n.*143C>G
|
|
ENST00000368485.7:c.1335C>G
|
ENSP00000357470.3:p.His445Gln
|
|
ENST00000507256.1:n.533C>G
|
|
|
NM_000565.3:c.1335C>G
|
NP_000556.1:p.His445Gln
|
|
NM_181359.2:c.*143C>G
|
NP_852004.1:n.*143C>G
|
|
XM_005245139.1:c.*16C>G
|
XP_005245196.1:n.*16C>G
|
|
XM_005245140.1:c.*176C>G
|
XP_005245197.1:n.*176C>G
|
|
XM_006711298.1:c.1383C>G
|
XP_006711361.1:p.His461Gln
|
|
XM_005245139.2:c.*16C>G
|
XP_005245196.1:n.*16C>G
|
|
XM_005245140.3:c.*176C>G
|
XP_005245197.1:n.*176C>G
|
|
XM_006711298.2:c.1383C>G
|
XP_006711361.1:p.His461Gln
|
|
XM_017001199.2:c.1482C>G
|
XP_016856688.1:p.His494Gln
|
|
XM_017001200.2:c.1434C>G
|
XP_016856689.1:p.His478Gln
|
|
XM_017001201.2:c.*176C>G
|
XP_016856690.1:n.*176C>G
|
|
NM_000565.4:c.1335C>G
MANE Select
|
NP_000556.1:p.His445Gln
|
|
NM_181359.3:c.*143C>G
|
NP_852004.1:n.*143C>G
|
|
NM_001382769.1:c.1434C>G
|
NP_001369698.1:p.His478Gln
|
|
NM_001382770.1:c.1428C>G
|
NP_001369699.1:p.His476Gln
|
|
NM_001382771.1:c.1383C>G
|
NP_001369700.1:p.His461Gln
|
|
NM_001382772.1:c.1329C>G
|
NP_001369701.1:p.His443Gln
|
|
NM_001382773.1:c.*143C>G
|
NP_001369702.1:n.*143C>G
|
|
NM_001382774.1:c.975C>G
|
NP_001369703.1:p.His325Gln
|
|