ENST00000350051.8:c.408G>T
MANE Select
|
ENSP00000324180.4:p.Glu136Asp
|
|
ENST00000301633.8:c.477G>T
|
ENSP00000301633.3:p.Glu159Asp
|
|
ENST00000350051.7:c.408G>T
|
ENSP00000324180.4:p.Glu136Asp
|
|
ENST00000374948.6:c.290G>T
|
ENSP00000364086.1:p.Ser97Ile
|
|
ENST00000589892.1:n.424G>T
|
|
|
ENST00000590925.6:c.*210G>T
|
ENSP00000467336.1:n.*210G>T
|
|
NM_001012270.1:c.290G>T
|
NP_001012270.1:p.Ser97Ile
|
|
NM_001012271.1:c.477G>T
|
NP_001012271.1:p.Glu159Asp
|
|
NM_001168.2:c.408G>T
|
NP_001159.2:p.Glu136Asp
|
|
XR_243654.3:n.610G>T
|
|
|
XR_934452.1:n.679G>T
|
|
|
XR_243654.5:n.610G>T
|
|
|
XR_934452.3:n.679G>T
|
|
|
NM_001168.3:c.408G>T
MANE Select
|
NP_001159.2:p.Glu136Asp
|
|
NM_001012270.2:c.290G>T
|
NP_001012270.1:p.Ser97Ile
|
|
NM_001012271.2:c.477G>T
|
NP_001012271.1:p.Glu159Asp
|
|