|
ENST00000342771.10:c.834G>T
MANE Select
|
ENSP00000344087.4:p.Gln278His
|
|
|
ENST00000443672.2:c.-197-3153G>T
|
ENSP00000393548.2:n.-197-3153G>T
|
|
|
ENST00000644359.1:c.-538G>T
|
ENSP00000494561.1:n.-538G>T
|
|
|
ENST00000644506.1:c.-538G>T
|
ENSP00000496672.1:n.-538G>T
|
|
|
ENST00000644939.1:c.834G>T
|
ENSP00000496726.1:p.Gln278His
|
|
|
ENST00000656200.1:c.-541G>T
|
ENSP00000499508.1:n.-541G>T
|
|
|
ENST00000342771.8:c.834G>T
|
ENSP00000344087.4:p.Gln278His
|
|
|
ENST00000406775.6:c.834G>T
|
ENSP00000385263.2:p.Gln278His
|
|
|
ENST00000416482.1:c.175G>T
|
|
|
|
ENST00000611706.4:c.90G>T
|
ENSP00000478134.1:p.Gln30His
|
|
|
ENST00000615871.4:c.90G>T
|
ENSP00000479325.1:p.Gln30His
|
|
|
NM_001127231.2:c.834G>T
|
NP_001120703.1:p.Gln278His
|
|
|
NM_015570.3:c.834G>T
|
NP_056385.1:p.Gln278His
|
|
|
XM_011516010.1:c.834G>T
|
XP_011514312.1:p.Gln278His
|
|
|
XM_011516011.1:c.834G>T
|
XP_011514313.1:p.Gln278His
|
|
|
XM_011516012.1:c.834G>T
|
XP_011514314.1:p.Gln278His
|
|
|
XM_011516013.1:c.834G>T
|
XP_011514315.1:p.Gln278His
|
|
|
XM_011516014.1:c.834G>T
|
XP_011514316.1:p.Gln278His
|
|
|
XM_011516015.1:c.834G>T
|
XP_011514317.1:p.Gln278His
|
|
|
XM_011516016.1:c.543G>T
|
XP_011514318.1:p.Gln181His
|
|
|
XM_011516017.1:c.360G>T
|
XP_011514319.1:p.Gln120His
|
|
|
XM_011516018.1:c.333G>T
|
XP_011514320.1:p.Gln111His
|
|
|
XM_011516010.2:c.834G>T
|
XP_011514312.1:p.Gln278His
|
|
|
XM_011516011.2:c.834G>T
|
XP_011514313.1:p.Gln278His
|
|
|
XM_011516012.2:c.834G>T
|
XP_011514314.1:p.Gln278His
|
|
|
XM_011516013.2:c.834G>T
|
XP_011514315.1:p.Gln278His
|
|
|
XM_011516014.2:c.834G>T
|
XP_011514316.1:p.Gln278His
|
|
|
XM_011516017.2:c.360G>T
|
XP_011514319.1:p.Gln120His
|
|
|
XM_011516018.2:c.333G>T
|
XP_011514320.1:p.Gln111His
|
|
|
XM_017011951.2:c.834G>T
|
XP_016867440.1:p.Gln278His
|
|
|
NM_001127231.3:c.834G>T
|
NP_001120703.1:p.Gln278His
|
|
|
NM_015570.4:c.834G>T
MANE Select
|
NP_056385.1:p.Gln278His
|
|
