ENST00000367698.4:c.1299T>A
MANE Select
|
ENSP00000356671.3:p.Thr433=
|
|
ENST00000367698.3:c.1299T>A
|
ENSP00000356671.3:p.Thr433=
|
|
ENST00000617423.4:c.684T>A
|
ENSP00000478688.1:p.Thr228=
|
|
NM_000488.3:c.1299T>A , LRG_577t1:c.1299T>A
|
NP_000479.1:p.Thr433=
|
|
XM_005245198.2:c.1155T>A
|
XP_005245255.1:p.Thr385=
|
|
NM_001365052.1:c.1155T>A
|
NP_001351981.1:p.Thr385=
|
|
NM_000488.4:c.1299T>A
MANE Select
|
NP_000479.1:p.Thr433=
|
|
NM_001365052.2:c.1155T>A
|
NP_001351981.1:p.Thr385=
|
|
NM_001386302.1:c.1422T>A
|
NP_001373231.1:p.Thr474=
|
|
NM_001386303.1:c.1380T>A
|
NP_001373232.1:p.Thr460=
|
|
NM_001386304.1:c.1278T>A
|
NP_001373233.1:p.Thr426=
|
|
NM_001386305.1:c.1242T>A
|
NP_001373234.1:p.Thr414=
|
|
NM_001386306.1:c.1083T>A
|
NP_001373235.1:p.Thr361=
|
|