ENST00000700075.1:c.63G>C
|
ENSP00000514784.1:p.Gln21His
|
|
ENST00000342771.10:c.1995G>C
MANE Select
|
ENSP00000344087.4:p.Gln665His
|
|
ENST00000439256.2:c.93G>C
|
ENSP00000407058.2:p.Gln31His
|
|
ENST00000443672.2:c.330G>C
|
ENSP00000393548.2:p.Gln110His
|
|
ENST00000449547.6:c.88G>C
|
|
|
ENST00000464768.2:n.663G>C
|
|
|
ENST00000644359.1:c.576G>C
|
ENSP00000494561.1:p.Gln192His
|
|
ENST00000644506.1:c.621G>C
|
ENSP00000496672.1:p.Gln207His
|
|
ENST00000644939.1:c.1992G>C
|
ENSP00000496726.1:p.Gln664His
|
|
ENST00000646136.1:n.306G>C
|
|
|
ENST00000647140.1:c.860G>C
|
|
|
ENST00000342771.8:c.1995G>C
|
ENSP00000344087.4:p.Gln665His
|
|
ENST00000406775.6:c.1923G>C
|
ENSP00000385263.2:p.Gln641His
|
|
ENST00000439256.1:c.93G>C
|
|
|
ENST00000464768.1:n.661G>C
|
|
|
ENST00000465899.1:n.492G>C
|
|
|
ENST00000498384.5:n.363G>C
|
|
|
ENST00000611706.4:c.1251G>C
|
ENSP00000478134.1:p.Gln417His
|
|
ENST00000615871.4:c.1179G>C
|
ENSP00000479325.1:p.Gln393His
|
|
NM_001127231.2:c.1923G>C
|
NP_001120703.1:p.Gln641His
|
|
NM_015570.3:c.1995G>C
|
NP_056385.1:p.Gln665His
|
|
XM_005250257.1:c.642G>C
|
XP_005250314.1:p.Gln214His
|
|
XM_011516010.1:c.2016G>C
|
XP_011514312.1:p.Gln672His
|
|
XM_011516011.1:c.2013G>C
|
XP_011514313.1:p.Gln671His
|
|
XM_011516012.1:c.1950G>C
|
XP_011514314.1:p.Gln650His
|
|
XM_011516013.1:c.1944G>C
|
XP_011514315.1:p.Gln648His
|
|
XM_011516014.1:c.1914G>C
|
XP_011514316.1:p.Gln638His
|
|
XM_011516015.1:c.1752G>C
|
XP_011514317.1:p.Gln584His
|
|
XM_011516016.1:c.1725G>C
|
XP_011514318.1:p.Gln575His
|
|
XM_011516017.1:c.1542G>C
|
XP_011514319.1:p.Gln514His
|
|
XM_011516018.1:c.1515G>C
|
XP_011514320.1:p.Gln505His
|
|
XM_005250257.2:c.642G>C
|
XP_005250314.1:p.Gln214His
|
|
XM_011516010.2:c.2016G>C
|
XP_011514312.1:p.Gln672His
|
|
XM_011516011.2:c.2013G>C
|
XP_011514313.1:p.Gln671His
|
|
XM_011516012.2:c.1950G>C
|
XP_011514314.1:p.Gln650His
|
|
XM_011516013.2:c.1944G>C
|
XP_011514315.1:p.Gln648His
|
|
XM_011516014.2:c.1914G>C
|
XP_011514316.1:p.Gln638His
|
|
XM_011516017.2:c.1542G>C
|
XP_011514319.1:p.Gln514His
|
|
XM_011516018.2:c.1515G>C
|
XP_011514320.1:p.Gln505His
|
|
XM_017011951.2:c.2016G>C
|
XP_016867440.1:p.Gln672His
|
|
NM_001127231.3:c.1923G>C
|
NP_001120703.1:p.Gln641His
|
|
NM_015570.4:c.1995G>C
MANE Select
|
NP_056385.1:p.Gln665His
|
|