|
ENST00000367698.4:c.895A=
MANE Select
|
ENSP00000356671.3:p.Thr299=
|
|
|
ENST00000367698.3:c.895A=
|
ENSP00000356671.3:p.Thr299=
|
|
|
ENST00000487183.1:n.546A=
|
|
|
|
ENST00000617423.4:c.559+2054A=
|
ENSP00000478688.1:n.559+2054A=
|
|
|
NM_000488.3:c.895A= , LRG_577t1:c.895A=
|
NP_000479.1:p.Thr299=
|
|
|
XM_005245198.2:c.751A=
|
XP_005245255.1:p.Thr251=
|
|
|
NM_001365052.1:c.751A=
|
NP_001351981.1:p.Thr251=
|
|
|
NM_000488.4:c.895A=
MANE Select
|
NP_000479.1:p.Thr299=
|
|
|
NM_001365052.2:c.751A=
|
NP_001351981.1:p.Thr251=
|
|
|
NM_001386302.1:c.1018A=
|
NP_001373231.1:p.Thr340=
|
|
|
NM_001386303.1:c.976A=
|
NP_001373232.1:p.Thr326=
|
|
|
NM_001386304.1:c.874A=
|
NP_001373233.1:p.Thr292=
|
|
|
NM_001386305.1:c.838A=
|
NP_001373234.1:p.Thr280=
|
|
|
NM_001386306.1:c.679A=
|
NP_001373235.1:p.Thr227=
|
|
