ENST00000318312.12:c.483G>C
MANE Select
|
ENSP00000317469.7:p.Glu161Asp
|
|
ENST00000318312.11:c.483G>C
|
ENSP00000317469.7:p.Glu161Asp
|
|
ENST00000393994.4:c.483G>C
|
ENSP00000377563.2:p.Glu161Asp
|
|
ENST00000419755.3:c.594G>C
|
ENSP00000398526.3:p.Glu198Asp
|
|
ENST00000455748.6:c.432+1018G>C
|
ENSP00000405764.2:n.432+1018G>C
|
|
ENST00000524458.5:c.*143G>C
|
ENSP00000436195.1:n.*143G>C
|
|
ENST00000524907.5:n.579G>C
|
|
|
ENST00000525809.5:c.210G>C
|
ENSP00000431187.1:p.Glu70Asp
|
|
ENST00000526035.5:c.*190G>C
|
ENSP00000434197.1:n.*190G>C
|
|
ENST00000526760.5:c.*190G>C
|
ENSP00000432140.1:n.*190G>C
|
|
ENST00000527251.5:c.*190G>C
|
ENSP00000434360.1:n.*190G>C
|
|
ENST00000528543.1:n.5G>C
|
|
|
ENST00000529766.5:n.490G>C
|
|
|
ENST00000529953.5:n.135G>C
|
|
|
ENST00000529955.5:n.454G>C
|
|
|
ENST00000532908.5:c.*143G>C
|
ENSP00000431866.1:n.*143G>C
|
|
ENST00000533430.5:n.261G>C
|
|
|
ENST00000533557.5:c.*143G>C
|
ENSP00000434619.1:n.*143G>C
|
|
ENST00000533644.5:c.436G>C
|
ENSP00000436073.1:p.Asp146His
|
|
ENST00000534730.5:n.495G>C
|
|
|
ENST00000630659.2:c.*190G>C
|
ENSP00000486455.1:n.*190G>C
|
|
NM_024649.4:c.483G>C
|
NP_078925.3:p.Glu161Asp
|
|
NM_024649.5:c.483G>C
MANE Select
|
NP_078925.3:p.Glu161Asp
|
|