ENST00000337299.7:c.86-1628C>A
|
ENSP00000338213.6:n.86-1628C>A
|
|
ENST00000380518.8:c.152C>A
MANE Select
|
ENSP00000369889.3:p.Pro51His
|
|
ENST00000490609.2:n.385C>A
|
|
|
ENST00000337299.6:c.86-1628C>A
|
ENSP00000338213.6:n.86-1628C>A
|
|
ENST00000380518.7:c.152C>A
|
ENSP00000369889.3:p.Pro51His
|
|
ENST00000474996.6:n.390C>A
|
|
|
ENST00000490609.1:n.317C>A
|
|
|
NM_001844.4:c.152C>A
|
NP_001835.3:p.Pro51His
|
|
NM_033150.2:c.86-1628C>A
|
NP_149162.2:n.86-1628C>A
|
|
XM_006719242.2:c.293C>A
|
XP_006719305.2:p.Pro98His
|
|
XM_011537928.1:c.293C>A
|
XP_011536230.1:p.Pro98His
|
|
XM_011537929.1:c.293C>A
|
XP_011536231.1:p.Pro98His
|
|
XM_011537930.1:c.293C>A
|
XP_011536232.1:p.Pro98His
|
|
XM_011537931.1:c.293C>A
|
XP_011536233.1:p.Pro98His
|
|
XM_011537932.1:c.293C>A
|
XP_011536234.1:p.Pro98His
|
|
XM_011537933.1:c.293C>A
|
XP_011536235.1:p.Pro98His
|
|
XM_011537934.1:c.293C>A
|
XP_011536236.1:p.Pro98His
|
|
XM_017018828.1:c.293C>A
|
XP_016874317.1:p.Pro98His
|
|
XM_017018829.1:c.293C>A
|
XP_016874318.1:p.Pro98His
|
|
XM_017018830.1:c.227-1628C>A
|
XP_016874319.1:n.227-1628C>A
|
|
XM_017018831.2:c.-395C>A
|
XP_016874320.1:n.-395C>A
|
|
NM_001844.5:c.152C>A
MANE Select
|
NP_001835.3:p.Pro51His
|
|
NM_033150.3:c.86-1628C>A
|
NP_149162.2:n.86-1628C>A
|
|