ENST00000409367.6:c.66G>T
|
ENSP00000387274.1:p.Gln22His
|
|
ENST00000416246.6:c.66G>T
|
ENSP00000408164.2:p.Gln22His
|
|
ENST00000698074.1:c.66G>T
|
ENSP00000513546.1:p.Gln22His
|
|
ENST00000698075.1:c.66G>T
|
ENSP00000513547.1:p.Gln22His
|
|
ENST00000698076.1:c.66G>T
|
ENSP00000513548.1:p.Gln22His
|
|
ENST00000698077.1:c.186G>T
|
ENSP00000513549.1:p.Gln62His
|
|
ENST00000698078.1:c.186G>T
|
ENSP00000513550.1:p.Gln62His
|
|
ENST00000698079.1:c.186G>T
|
ENSP00000513551.1:p.Gln62His
|
|
ENST00000698080.1:c.186G>T
|
ENSP00000513552.1:p.Gln62His
|
|
ENST00000698081.1:c.186G>T
|
ENSP00000513553.1:p.Gln62His
|
|
ENST00000698082.1:n.295G>T
|
|
|
ENST00000698083.1:c.186G>T
|
ENSP00000513554.1:p.Gln62His
|
|
ENST00000698084.1:c.66G>T
|
ENSP00000513555.1:p.Gln22His
|
|
ENST00000698085.1:n.282G>T
|
|
|
ENST00000698086.1:c.186G>T
|
ENSP00000513556.1:p.Gln62His
|
|
ENST00000698087.1:c.186G>T
|
ENSP00000513557.1:p.Gln62His
|
|
ENST00000698088.1:c.186G>T
|
ENSP00000513558.1:p.Gln62His
|
|
ENST00000698089.1:c.66G>T
|
ENSP00000513559.1:p.Gln22His
|
|
ENST00000698090.1:c.186G>T
|
ENSP00000513560.1:p.Gln62His
|
|
ENST00000698091.1:n.2046G>T
|
|
|
ENST00000698092.1:n.42G>T
|
|
|
ENST00000338523.9:c.186G>T
MANE Select
|
ENSP00000343709.5:p.Gln62His
|
|
ENST00000338523.8:c.186G>T
|
ENSP00000343709.4:p.Gln62His
|
|
ENST00000396376.5:c.186G>T
|
ENSP00000379661.1:p.Gln62His
|
|
ENST00000409367.5:c.66G>T
|
ENSP00000387274.1:p.Gln22His
|
|
ENST00000409838.1:c.-41+107G>T
|
ENSP00000386540.1:n.-41+107G>T
|
|
ENST00000416246.5:c.264G>T
|
ENSP00000408164.1:p.Gln88His
|
|
ENST00000446848.6:c.186G>T
|
ENSP00000395474.3:p.Gln62His
|
|
ENST00000619420.4:c.186G>T
|
ENSP00000478710.1:p.Gln62His
|
|
NM_001199835.1:c.186G>T
|
NP_001186764.1:p.Gln62His
|
|
NM_001199837.1:c.177G>T
|
NP_001186766.1:p.Gln59His
|
|
NM_001199838.1:c.-41+107G>T
|
NP_001186767.1:n.-41+107G>T
|
|
NM_013322.2:c.186G>T
|
NP_037454.2:p.Gln62His
|
|
NR_037670.1:n.522G>T
|
|
|
XM_006715710.1:c.186G>T
|
XP_006715773.1:p.Gln62His
|
|
XM_006715711.1:c.186G>T
|
XP_006715774.1:p.Gln62His
|
|
XM_006715712.1:c.186G>T
|
XP_006715775.1:p.Gln62His
|
|
NM_001318198.1:c.264G>T
|
NP_001305127.1:p.Gln88His
|
|
NM_001318199.1:c.186G>T
|
NP_001305128.1:p.Gln62His
|
|
NM_001362753.1:c.264G>T
|
NP_001349682.1:p.Gln88His
|
|
NM_001362754.1:c.264G>T
|
NP_001349683.1:p.Gln88His
|
|
XM_006715712.2:c.186G>T
|
XP_006715775.1:p.Gln62His
|
|
XM_017012086.1:c.264G>T
|
XP_016867575.1:p.Gln88His
|
|
NM_001199837.2:c.177G>T
|
NP_001186766.1:p.Gln59His
|
|
NM_001318199.2:c.186G>T
|
NP_001305128.1:p.Gln62His
|
|
NM_013322.3:c.186G>T
MANE Select
|
NP_037454.2:p.Gln62His
|
|
NM_001199837.3:c.177G>T
|
NP_001186766.1:p.Gln59His
|
|
NM_001199838.2:c.-41+107G>T
|
NP_001186767.1:n.-41+107G>T
|
|
NM_001318199.3:c.186G>T
|
NP_001305128.1:p.Gln62His
|
|