ENST00000397120.8:c.1161G>T
(AP1G2)
MANE Select
|
ENSP00000380309.3:p.Gln387His
|
|
ENST00000308724.9:c.1161G>T
(AP1G2)
|
ENSP00000312442.5:p.Gln387His
|
|
ENST00000397120.7:c.1161G>T
(AP1G2)
|
ENSP00000380309.3:p.Gln387His
|
|
ENST00000460049.6:n.1334G>T
(AP1G2)
|
|
|
ENST00000465445.6:n.1220G>T
(AP1G2)
|
|
|
ENST00000535852.6:n.1101G>T
(AP1G2)
|
|
|
ENST00000554554.5:n.163G>T
(AP1G2)
|
|
|
ENST00000554977.1:n.478G>T
(AP1G2)
|
|
|
ENST00000554982.5:n.67G>T
(AP1G2)
|
|
|
ENST00000555118.1:n.5G>T
(AP1G2)
|
|
|
ENST00000555789.5:n.110G>T
(AP1G2)
|
|
|
ENST00000555974.1:n.116G>T
(AP1G2)
|
|
|
ENST00000556741.5:n.120G>T
(AP1G2)
|
|
|
ENST00000557162.1:c.310G>T
(AP1G2)
|
|
|
NM_001282474.1:c.18G>T
(AP1G2)
|
NP_001269403.1:p.Gln6His
|
|
NM_001282475.1:c.945G>T
(AP1G2)
|
NP_001269404.1:p.Gln315His
|
|
NM_003917.4:c.1161G>T
(AP1G2)
|
NP_003908.1:p.Gln387His
|
|
NR_110555.1:n.778-940C>A
(AP1G2-AS1)
|
|
|
XM_005268167.2:c.1332G>T
(AP1G2)
|
XP_005268224.1:p.Gln444His
|
|
XM_005268168.3:c.1332G>T
(AP1G2)
|
XP_005268225.1:p.Gln444His
|
|
XM_005268169.2:c.1332G>T
(AP1G2)
|
XP_005268226.1:p.Gln444His
|
|
XM_005268170.2:c.1332G>T
(AP1G2)
|
XP_005268227.1:p.Gln444His
|
|
XM_005268172.2:c.1161G>T
(AP1G2)
|
XP_005268229.1:p.Gln387His
|
|
XM_005268173.2:c.1161G>T
(AP1G2)
|
XP_005268230.1:p.Gln387His
|
|
XM_005268174.2:c.945G>T
(AP1G2)
|
XP_005268231.1:p.Gln315His
|
|
XM_005268175.2:c.945G>T
(AP1G2)
|
XP_005268232.1:p.Gln315His
|
|
XM_005268177.2:c.774G>T
(AP1G2)
|
XP_005268234.1:p.Gln258His
|
|
XM_005268178.2:c.774G>T
(AP1G2)
|
XP_005268235.1:p.Gln258His
|
|
XM_005268179.2:c.774G>T
(AP1G2)
|
XP_005268236.1:p.Gln258His
|
|
XM_005268180.3:c.726G>T
(AP1G2)
|
XP_005268237.1:p.Gln242His
|
|
XM_005268181.2:c.1434G>T
(AP1G2)
|
XP_005268238.1:p.Gln478His
|
|
XM_005268182.2:c.531G>T
(AP1G2)
|
XP_005268239.1:p.Gln177His
|
|
XM_006720301.2:c.1332G>T
(AP1G2)
|
XP_006720364.1:p.Gln444His
|
|
XM_011537282.1:c.1332G>T
(AP1G2)
|
XP_011535584.1:p.Gln444His
|
|
XM_011537283.1:c.1332G>T
(AP1G2)
|
XP_011535585.1:p.Gln444His
|
|
XM_011537284.1:c.1434G>T
(AP1G2)
|
XP_011535586.1:p.Gln478His
|
|
XM_011537285.1:c.1434G>T
(AP1G2)
|
XP_011535587.1:p.Gln478His
|
|
XM_011537286.1:c.18G>T
(AP1G2)
|
XP_011535588.1:p.Gln6His
|
|
XR_943550.1:n.1333G>T
(AP1G2)
|
|
|
XR_943551.1:n.1473G>T
(AP1G2)
|
|
|
XR_943552.1:n.1473G>T
(AP1G2)
|
|
|
XR_943553.1:n.1333G>T
(AP1G2)
|
|
|
XR_943554.1:n.1584G>T
(AP1G2)
|
|
|
XR_943555.1:n.1395G>T
(AP1G2)
|
|
|
NM_001354673.1:c.774G>T
(AP1G2)
|
NP_001341602.1:p.Gln258His
|
|
NM_001354674.1:c.18G>T
(AP1G2)
|
NP_001341603.1:p.Gln6His
|
|
NM_001354675.1:c.18G>T
(AP1G2)
|
NP_001341604.1:p.Gln6His
|
|
NM_001354677.1:c.18G>T
(AP1G2)
|
NP_001341606.1:p.Gln6His
|
|
NM_001354681.1:c.18G>T
(AP1G2)
|
NP_001341610.1:p.Gln6His
|
|
NR_148937.1:n.1589G>T
(AP1G2)
|
|
|
NR_148938.1:n.1390G>T
(AP1G2)
|
|
|
XM_005268167.3:c.1332G>T
(AP1G2)
|
XP_005268224.1:p.Gln444His
|
|
XM_005268168.5:c.1332G>T
(AP1G2)
|
XP_005268225.1:p.Gln444His
|
|
XM_005268169.3:c.1332G>T
(AP1G2)
|
XP_005268226.1:p.Gln444His
|
|
XM_005268170.3:c.1332G>T
(AP1G2)
|
XP_005268227.1:p.Gln444His
|
|
XM_005268172.3:c.1161G>T
(AP1G2)
|
XP_005268229.1:p.Gln387His
|
|
XM_005268173.3:c.1161G>T
(AP1G2)
|
XP_005268230.1:p.Gln387His
|
|
XM_005268174.3:c.945G>T
(AP1G2)
|
XP_005268231.1:p.Gln315His
|
|
XM_005268175.3:c.945G>T
(AP1G2)
|
XP_005268232.1:p.Gln315His
|
|
XM_005268178.4:c.774G>T
(AP1G2)
|
XP_005268235.1:p.Gln258His
|
|
XM_005268179.3:c.774G>T
(AP1G2)
|
XP_005268236.1:p.Gln258His
|
|
XM_005268180.4:c.726G>T
(AP1G2)
|
XP_005268237.1:p.Gln242His
|
|
XM_005268182.3:c.531G>T
(AP1G2)
|
XP_005268239.1:p.Gln177His
|
|
XM_006720301.3:c.1332G>T
(AP1G2)
|
XP_006720364.1:p.Gln444His
|
|
XM_011537283.3:c.1332G>T
(AP1G2)
|
XP_011535585.1:p.Gln444His
|
|
XM_017021740.1:c.1332G>T
(AP1G2)
|
XP_016877229.1:p.Gln444His
|
|
XM_017021741.1:c.1191G>T
(AP1G2)
|
XP_016877230.1:p.Gln397His
|
|
XM_017021742.2:c.945G>T
(AP1G2)
|
XP_016877231.1:p.Gln315His
|
|
XM_017021745.1:c.1161G>T
(AP1G2)
|
XP_016877234.1:p.Gln387His
|
|
XM_024449738.1:c.18G>T
(AP1G2)
|
XP_024305506.1:p.Gln6His
|
|
XR_001750583.2:n.1333G>T
(AP1G2)
|
|
|
XR_001750584.2:n.1333G>T
(AP1G2)
|
|
|
XR_001750586.1:n.1333G>T
(AP1G2)
|
|
|
XR_001750587.1:n.1333G>T
(AP1G2)
|
|
|
XR_001750588.2:n.1786G>T
(AP1G2)
|
|
|
XR_001750589.1:n.1584G>T
(AP1G2)
|
|
|
XR_001750590.2:n.1395G>T
(AP1G2)
|
|
|
XR_002957567.1:n.1333G>T
(AP1G2)
|
|
|
XR_002957568.1:n.1302G>T
(AP1G2)
|
|
|
XR_002957569.1:n.1216G>T
(AP1G2)
|
|
|
XR_002957570.1:n.1584G>T
(AP1G2)
|
|
|
NM_001282474.2:c.18G>T
(AP1G2)
|
NP_001269403.1:p.Gln6His
|
|
NM_001282475.2:c.945G>T
(AP1G2)
|
NP_001269404.1:p.Gln315His
|
|
NM_001354673.2:c.774G>T
(AP1G2)
|
NP_001341602.1:p.Gln258His
|
|
NM_001354674.2:c.18G>T
(AP1G2)
|
NP_001341603.1:p.Gln6His
|
|
NM_001354675.2:c.18G>T
(AP1G2)
|
NP_001341604.1:p.Gln6His
|
|
NM_001354677.2:c.18G>T
(AP1G2)
|
NP_001341606.1:p.Gln6His
|
|
NM_001354681.2:c.18G>T
(AP1G2)
|
NP_001341610.1:p.Gln6His
|
|
NM_003917.5:c.1161G>T
(AP1G2)
MANE Select
|
NP_003908.1:p.Gln387His
|
|
NR_148937.2:n.1867G>T
(AP1G2)
|
|
|
NR_148938.2:n.1393G>T
(AP1G2)
|
|
|