ENST00000539215.6:c.487T>G
|
|
|
ENST00000699982.1:c.1586T>G
|
|
|
ENST00000699983.1:c.1586T>G
|
|
|
ENST00000699984.1:c.1586T>G
|
|
|
ENST00000320574.10:c.1732T>G
MANE Select
|
ENSP00000322570.5:p.Leu578Val
|
|
ENST00000672742.1:c.*1234T>G
|
ENSP00000500279.1:n.*1234T>G
|
|
ENST00000320574.9:c.1732T>G
|
ENSP00000322570.5:p.Leu578Val
|
|
ENST00000535270.5:c.1651T>G
|
ENSP00000445753.1:p.Leu551Val
|
|
ENST00000537064.5:c.*779T>G
|
ENSP00000442578.1:n.*779T>G
|
|
NM_006231.3:c.1732T>G , LRG_789t1:c.1732T>G
|
NP_006222.2:p.Leu578Val
|
|
XM_011534795.1:c.1732T>G
|
XP_011533097.1:p.Leu578Val
|
|
XM_011534796.1:c.1603T>G
|
XP_011533098.1:p.Leu535Val
|
|
XM_011534797.1:c.811T>G
|
XP_011533099.1:p.Leu271Val
|
|
XM_011534798.1:c.394T>G
|
XP_011533100.1:p.Leu132Val
|
|
XM_011534799.1:c.1732T>G
|
XP_011533101.1:p.Leu578Val
|
|
XM_011534800.1:c.1732T>G
|
XP_011533102.1:p.Leu578Val
|
|
XM_011534801.1:c.1732T>G
|
XP_011533103.1:p.Leu578Val
|
|
XR_941395.1:n.1941T>G
|
|
|
XM_011534795.3:c.1732T>G
|
XP_011533097.1:p.Leu578Val
|
|
XM_011534797.3:c.811T>G
|
XP_011533099.1:p.Leu271Val
|
|
XM_011534799.2:c.1732T>G
|
XP_011533101.1:p.Leu578Val
|
|
XR_002957338.1:n.1936T>G
|
|
|
XR_002957339.1:n.1936T>G
|
|
|
XR_941395.2:n.1936T>G
|
|
|
NM_006231.4:c.1732T>G
MANE Select
|
NP_006222.2:p.Leu578Val
|
|