ENST00000539215.6:c.137T>A
|
|
|
ENST00000545015.2:n.1456T>A
|
|
|
ENST00000699982.1:c.1283T>A
|
|
|
ENST00000699983.1:c.1283T>A
|
|
|
ENST00000699984.1:c.1283T>A
|
|
|
ENST00000320574.10:c.1429T>A
MANE Select
|
ENSP00000322570.5:p.Phe477Ile
|
|
ENST00000672742.1:c.*931T>A
|
ENSP00000500279.1:n.*931T>A
|
|
ENST00000320574.9:c.1429T>A
|
ENSP00000322570.5:p.Phe477Ile
|
|
ENST00000535270.5:c.1348T>A
|
ENSP00000445753.1:p.Phe450Ile
|
|
ENST00000535934.2:n.1304T>A
|
|
|
ENST00000537064.5:c.*476T>A
|
ENSP00000442578.1:n.*476T>A
|
|
ENST00000539215.5:n.137T>A
|
|
|
ENST00000545015.1:n.26T>A
|
|
|
NM_006231.3:c.1429T>A , LRG_789t1:c.1429T>A
|
NP_006222.2:p.Phe477Ile
|
|
XM_011534795.1:c.1429T>A
|
XP_011533097.1:p.Phe477Ile
|
|
XM_011534796.1:c.1300T>A
|
XP_011533098.1:p.Phe434Ile
|
|
XM_011534797.1:c.508T>A
|
XP_011533099.1:p.Phe170Ile
|
|
XM_011534798.1:c.91T>A
|
XP_011533100.1:p.Phe31Ile
|
|
XM_011534799.1:c.1429T>A
|
XP_011533101.1:p.Phe477Ile
|
|
XM_011534800.1:c.1429T>A
|
XP_011533102.1:p.Phe477Ile
|
|
XM_011534801.1:c.1429T>A
|
XP_011533103.1:p.Phe477Ile
|
|
XR_941395.1:n.1638T>A
|
|
|
XM_011534795.3:c.1429T>A
|
XP_011533097.1:p.Phe477Ile
|
|
XM_011534797.3:c.508T>A
|
XP_011533099.1:p.Phe170Ile
|
|
XM_011534799.2:c.1429T>A
|
XP_011533101.1:p.Phe477Ile
|
|
XR_002957338.1:n.1633T>A
|
|
|
XR_002957339.1:n.1633T>A
|
|
|
XR_941395.2:n.1633T>A
|
|
|
NM_006231.4:c.1429T>A
MANE Select
|
NP_006222.2:p.Phe477Ile
|
|