ENST00000318312.12:c.541G>A
MANE Select
|
ENSP00000317469.7:p.Glu181Lys
|
|
ENST00000318312.11:c.541G>A
|
ENSP00000317469.7:p.Glu181Lys
|
|
ENST00000393994.4:c.541G>A
|
ENSP00000377563.2:p.Glu181Lys
|
|
ENST00000419755.3:c.652G>A
|
ENSP00000398526.3:p.Glu218Lys
|
|
ENST00000455748.6:c.432+1205G>A
|
ENSP00000405764.2:n.432+1205G>A
|
|
ENST00000524458.5:c.*330G>A
|
ENSP00000436195.1:n.*330G>A
|
|
ENST00000524907.5:n.637G>A
|
|
|
ENST00000525809.5:c.268G>A
|
ENSP00000431187.1:p.Glu90Lys
|
|
ENST00000526035.5:c.*248G>A
|
ENSP00000434197.1:n.*248G>A
|
|
ENST00000526760.5:c.*248G>A
|
ENSP00000432140.1:n.*248G>A
|
|
ENST00000527251.5:c.*248G>A
|
ENSP00000434360.1:n.*248G>A
|
|
ENST00000528543.1:n.63G>A
|
|
|
ENST00000529766.5:n.548G>A
|
|
|
ENST00000529953.5:n.193G>A
|
|
|
ENST00000529955.5:n.512G>A
|
|
|
ENST00000532908.5:c.*201G>A
|
ENSP00000431866.1:n.*201G>A
|
|
ENST00000533430.5:n.319G>A
|
|
|
ENST00000533557.5:c.*201G>A
|
ENSP00000434619.1:n.*201G>A
|
|
ENST00000533644.5:c.494G>A
|
ENSP00000436073.1:p.Ter165=
|
|
ENST00000630659.2:c.*248G>A
|
ENSP00000486455.1:n.*248G>A
|
|
NM_024649.4:c.541G>A
|
NP_078925.3:p.Glu181Lys
|
|
NM_024649.5:c.541G>A
MANE Select
|
NP_078925.3:p.Glu181Lys
|
|