ENST00000707113.1:c.236C>A
|
ENSP00000516742.1:p.Pro79His
|
|
ENST00000707114.1:c.236C>A
|
ENSP00000516743.1:p.Pro79His
|
|
ENST00000707115.1:c.236C>A
|
ENSP00000516744.1:p.Pro79His
|
|
ENST00000707116.1:c.236C>A
|
ENSP00000516745.1:p.Pro79His
|
|
ENST00000517291.2:c.278C>A
|
ENSP00000429441.2:p.Pro93His
|
|
ENST00000524013.2:c.278C>A
|
ENSP00000430235.2:p.Pro93His
|
|
ENST00000621592.8:c.281C>A
MANE Select
|
ENSP00000478887.2:p.Pro94His
|
|
ENST00000651626.1:c.-65C>A
|
ENSP00000499182.1:n.-65C>A
|
|
ENST00000652288.1:c.236C>A
|
ENSP00000499105.1:p.Pro79His
|
|
ENST00000259523.10:c.236C>A
|
ENSP00000259523.6:p.Pro79His
|
|
ENST00000377970.6:c.236C>A
|
ENSP00000367207.3:p.Pro79His
|
|
ENST00000517291.1:c.278C>A
|
ENSP00000429441.1:p.Pro93His
|
|
ENST00000524013.1:c.278C>A
|
ENSP00000430235.1:p.Pro93His
|
|
ENST00000613283.1:c.281C>A
|
ENSP00000479618.1:p.Pro94His
|
|
ENST00000621592.5:c.281C>A
|
ENSP00000478887.1:p.Pro94His
|
|
NM_002467.4:c.281C>A
|
NP_002458.2:p.Pro94His
|
|
NM_001354870.1:c.278C>A
|
NP_001341799.1:p.Pro93His
|
|
NM_002467.5:c.281C>A
|
NP_002458.2:p.Pro94His
|
|
NM_002467.6:c.281C>A
MANE Select
|
NP_002458.2:p.Pro94His
|
|