ENST00000232607.7:c.424G>T
MANE Select
|
ENSP00000232607.2:p.Glu142Ter
|
|
ENST00000232607.6:c.424G>T
|
ENSP00000232607.2:p.Glu142Ter
|
|
ENST00000460034.5:c.*168G>T
|
ENSP00000420409.1:n.*168G>T
|
|
ENST00000462091.5:c.*96G>T
|
ENSP00000417893.1:n.*96G>T
|
|
ENST00000467167.5:c.*322G>T
|
ENSP00000419618.1:n.*322G>T
|
|
ENST00000474588.5:c.311-234G>T
|
ENSP00000420348.1:n.311-234G>T
|
|
ENST00000479719.5:c.424G>T
|
ENSP00000420754.1:p.Glu142Ter
|
|
ENST00000497791.5:c.*96G>T
|
ENSP00000419121.1:n.*96G>T
|
|
ENST00000498715.1:n.142G>T
|
|
|
NM_000373.3:c.424G>T
|
NP_000364.1:p.Glu142Ter
|
|
NR_033434.1:n.376G>T
|
|
|
NR_033437.1:n.629G>T
|
|
|
XR_001740253.2:n.454G>T
|
|
|
NM_000373.4:c.424G>T
MANE Select
|
NP_000364.1:p.Glu142Ter
|
|
NR_033434.2:n.290G>T
|
|
|
NR_033437.2:n.543G>T
|
|
|