|
ENST00000367698.4:c.969C=
MANE Select
|
ENSP00000356671.3:p.Ser323=
|
|
|
ENST00000367698.3:c.969C=
|
ENSP00000356671.3:p.Ser323=
|
|
|
ENST00000487183.1:n.620C=
|
|
|
|
ENST00000617423.4:c.559+2128C=
|
ENSP00000478688.1:n.559+2128C=
|
|
|
NM_000488.3:c.969C= , LRG_577t1:c.969C=
|
NP_000479.1:p.Ser323=
|
|
|
XM_005245198.2:c.825C=
|
XP_005245255.1:p.Ser275=
|
|
|
NM_001365052.1:c.825C=
|
NP_001351981.1:p.Ser275=
|
|
|
NM_000488.4:c.969C=
MANE Select
|
NP_000479.1:p.Ser323=
|
|
|
NM_001365052.2:c.825C=
|
NP_001351981.1:p.Ser275=
|
|
|
NM_001386302.1:c.1092C=
|
NP_001373231.1:p.Ser364=
|
|
|
NM_001386303.1:c.1050C=
|
NP_001373232.1:p.Ser350=
|
|
|
NM_001386304.1:c.948C=
|
NP_001373233.1:p.Ser316=
|
|
|
NM_001386305.1:c.912C=
|
NP_001373234.1:p.Ser304=
|
|
|
NM_001386306.1:c.753C=
|
NP_001373235.1:p.Ser251=
|
|
