|
ENST00000700029.2:c.1073A>G
|
ENSP00000514759.2:p.Lys358Arg
|
|
|
ENST00000710265.1:c.980A>G
|
ENSP00000518161.1:p.Lys327Arg
|
|
|
ENST00000472832.3:c.980A>G
|
ENSP00000483066.2:p.Lys327Arg
|
|
|
ENST00000688158.2:n.1715A>G
|
|
|
|
ENST00000688922.2:c.*810A>G
|
ENSP00000508742.2:n.*810A>G
|
|
|
ENST00000700021.1:c.935A>G
|
ENSP00000514757.1:p.Lys312Arg
|
|
|
ENST00000700022.1:c.*319A>G
|
ENSP00000514758.1:n.*319A>G
|
|
|
ENST00000700023.1:n.2138A>G
|
|
|
|
ENST00000700024.1:n.2372A>G
|
|
|
|
ENST00000700025.1:n.1749A>G
|
|
|
|
ENST00000700026.1:n.617A>G
|
|
|
|
ENST00000706954.1:c.980A>G
|
ENSP00000516674.1:p.Lys327Arg
|
|
|
ENST00000706955.1:c.*1015A>G
|
ENSP00000516675.1:n.*1015A>G
|
|
|
ENST00000686459.1:c.*566A>G
|
ENSP00000508909.1:n.*566A>G
|
|
|
ENST00000688158.1:c.*1091A>G
|
ENSP00000509254.1:n.*1091A>G
|
|
|
ENST00000688308.1:c.980A>G
|
ENSP00000508752.1:p.Lys327Arg
|
|
|
ENST00000688922.1:c.901A>G
|
|
|
|
ENST00000693560.1:c.1499A>G
|
ENSP00000509861.1:p.Lys500Arg
|
|
|
ENST00000371953.8:c.980A>G
MANE Select
|
ENSP00000361021.3:p.Lys327Arg
|
|
|
ENST00000371953.7:c.980A>G
|
ENSP00000361021.3:p.Lys327Arg
|
|
|
ENST00000472832.2:c.407A>G
|
ENSP00000483066.1:p.Lys136Arg
|
|
|
NM_000314.5:c.980A>G
|
NP_000305.3:p.Lys327Arg
|
|
|
NM_000314.6:c.980A>G
|
NP_000305.3:p.Lys327Arg
|
|
|
NM_001304717.2:c.1499A>G
|
NP_001291646.2:p.Lys500Arg
|
|
|
NM_001304718.1:c.389A>G
|
NP_001291647.1:p.Lys130Arg
|
|
|
XM_006717926.2:c.935A>G
|
XP_006717989.1:p.Lys312Arg
|
|
|
XM_011539981.1:c.980A>G
|
XP_011538283.1:p.Lys327Arg
|
|
|
XM_011539982.1:c.884A>G
|
XP_011538284.1:p.Lys295Arg
|
|
|
XR_945791.1:n.1550A>G
|
|
|
|
NM_000314.7:c.980A>G
|
NP_000305.3:p.Lys327Arg
|
|
|
NM_001304717.5:c.1499A>G
|
NP_001291646.4:p.Lys500Arg
|
|
|
NM_001304718.2:c.389A>G
|
NP_001291647.1:p.Lys130Arg
|
|
|
NM_000314.8:c.980A>G
MANE Select
|
NP_000305.3:p.Lys327Arg
|
|
