ENST00000367698.4:c.1324G>A
MANE Select
|
ENSP00000356671.3:p.Val442Ile
|
|
ENST00000367698.3:c.1324G>A
|
ENSP00000356671.3:p.Val442Ile
|
|
ENST00000617423.4:c.709G>A
|
ENSP00000478688.1:p.Val237Ile
|
|
NM_000488.3:c.1324G>A , LRG_577t1:c.1324G>A
|
NP_000479.1:p.Val442Ile
|
|
XM_005245198.2:c.1180G>A
|
XP_005245255.1:p.Val394Ile
|
|
NM_001365052.1:c.1180G>A
|
NP_001351981.1:p.Val394Ile
|
|
NM_000488.4:c.1324G>A
MANE Select
|
NP_000479.1:p.Val442Ile
|
|
NM_001365052.2:c.1180G>A
|
NP_001351981.1:p.Val394Ile
|
|
NM_001386302.1:c.1447G>A
|
NP_001373231.1:p.Val483Ile
|
|
NM_001386303.1:c.1405G>A
|
NP_001373232.1:p.Val469Ile
|
|
NM_001386304.1:c.1303G>A
|
NP_001373233.1:p.Val435Ile
|
|
NM_001386305.1:c.1267G>A
|
NP_001373234.1:p.Val423Ile
|
|
NM_001386306.1:c.1108G>A
|
NP_001373235.1:p.Val370Ile
|
|