ENST00000305264.8:c.966G=
MANE Select
|
ENSP00000302967.3:p.Glu322=
|
|
ENST00000305264.7:c.966G=
|
ENSP00000302967.3:p.Glu322=
|
|
ENST00000459727.5:n.233+168G=
|
|
|
ENST00000467533.5:n.599+168G=
|
|
|
ENST00000469207.5:n.45G=
|
|
|
ENST00000469550.6:n.1039G=
|
|
|
ENST00000475549.1:n.297G=
|
|
|
ENST00000486618.1:n.460G=
|
|
|
ENST00000491581.5:n.180G=
|
|
|
ENST00000492407.1:n.767+168G=
|
|
|
NM_003883.3:c.966G=
|
NP_003874.2:p.Glu322=
|
|
XM_011537697.1:c.405G=
|
XP_011535999.1:p.Glu135=
|
|
XR_944336.1:n.1051G=
|
|
|
NM_001355039.1:c.966G=
|
NP_001341968.1:p.Glu322=
|
|
NM_001355040.1:c.507G=
|
NP_001341969.1:p.Glu169=
|
|
NM_001355041.1:c.405G=
|
NP_001341970.1:p.Glu135=
|
|
NR_149164.1:n.1032G=
|
|
|
NR_149165.1:n.914G=
|
|
|
NR_149166.1:n.843+168G=
|
|
|
NR_149167.1:n.1011+168G=
|
|
|
NR_149168.1:n.1057G=
|
|
|
NR_149169.1:n.1057G=
|
|
|
NM_003883.4:c.966G=
MANE Select
|
NP_003874.2:p.Glu322=
|
|
NM_001355039.2:c.966G=
|
NP_001341968.1:p.Glu322=
|
|
NR_149167.2:n.1004+168G=
|
|
|
NM_001355040.2:c.507G=
|
NP_001341969.1:p.Glu169=
|
|
NM_001355041.2:c.405G=
|
NP_001341970.1:p.Glu135=
|
|
NR_149164.2:n.1025G=
|
|
|
NR_149165.2:n.907G=
|
|
|
NR_149166.2:n.836+168G=
|
|
|
NR_149168.2:n.1050G=
|
|
|
NR_149169.2:n.1050G=
|
|
|