ENST00000367698.4:c.1325T>A
MANE Select
|
ENSP00000356671.3:p.Val442Asp
|
|
ENST00000367698.3:c.1325T>A
|
ENSP00000356671.3:p.Val442Asp
|
|
ENST00000617423.4:c.710T>A
|
ENSP00000478688.1:p.Val237Asp
|
|
NM_000488.3:c.1325T>A , LRG_577t1:c.1325T>A
|
NP_000479.1:p.Val442Asp
|
|
XM_005245198.2:c.1181T>A
|
XP_005245255.1:p.Val394Asp
|
|
NM_001365052.1:c.1181T>A
|
NP_001351981.1:p.Val394Asp
|
|
NM_000488.4:c.1325T>A
MANE Select
|
NP_000479.1:p.Val442Asp
|
|
NM_001365052.2:c.1181T>A
|
NP_001351981.1:p.Val394Asp
|
|
NM_001386302.1:c.1448T>A
|
NP_001373231.1:p.Val483Asp
|
|
NM_001386303.1:c.1406T>A
|
NP_001373232.1:p.Val469Asp
|
|
NM_001386304.1:c.1304T>A
|
NP_001373233.1:p.Val435Asp
|
|
NM_001386305.1:c.1268T>A
|
NP_001373234.1:p.Val423Asp
|
|
NM_001386306.1:c.1109T>A
|
NP_001373235.1:p.Val370Asp
|
|