|
ENST00000341142.8:c.816G>A
(GMPPA)
|
ENSP00000340760.3:p.Arg272=
|
|
|
ENST00000435316.6:c.711G>A
(GMPPA)
|
ENSP00000411060.1:p.Arg237=
|
|
|
ENST00000455657.6:c.*91G>A
(GMPPA)
|
ENSP00000392465.3:n.*91G>A
|
|
|
ENST00000496536.2:n.825G>A
(GMPPA)
|
|
|
|
ENST00000622191.2:c.816G>A
(GMPPA)
|
ENSP00000478700.2:p.Arg272=
|
|
|
ENST00000682058.1:c.*847G>A
(GMPPA)
|
ENSP00000507378.1:n.*847G>A
|
|
|
ENST00000682102.1:c.756-82G>A
(GMPPA)
|
ENSP00000508279.1:n.756-82G>A
|
|
|
ENST00000682340.1:n.2290G>A
(GMPPA)
|
|
|
|
ENST00000682435.1:n.1400G>A
(GMPPA)
|
|
|
|
ENST00000682443.1:n.2102G>A
(GMPPA)
|
|
|
|
ENST00000682481.1:c.*1101G>A
(GMPPA)
|
ENSP00000507331.1:n.*1101G>A
|
|
|
ENST00000682488.1:c.70-1206G>A
(GMPPA)
|
ENSP00000507140.1:n.70-1206G>A
|
|
|
ENST00000682576.1:c.*787-82G>A
(GMPPA)
|
ENSP00000508370.1:n.*787-82G>A
|
|
|
ENST00000683106.1:n.1836G>A
(GMPPA)
|
|
|
|
ENST00000683131.1:c.*1101G>A
(GMPPA)
|
ENSP00000507530.1:n.*1101G>A
|
|
|
ENST00000683241.1:n.1181G>A
(GMPPA)
|
|
|
|
ENST00000683382.1:n.1919G>A
(GMPPA)
|
|
|
|
ENST00000683386.1:c.*446G>A
(GMPPA)
|
ENSP00000507844.1:n.*446G>A
|
|
|
ENST00000683402.1:c.*197G>A
(GMPPA)
|
ENSP00000507137.1:n.*197G>A
|
|
|
ENST00000683591.1:c.*847G>A
(GMPPA)
|
ENSP00000508406.1:n.*847G>A
|
|
|
ENST00000683598.1:c.*847G>A
(GMPPA)
|
ENSP00000508168.1:n.*847G>A
|
|
|
ENST00000683617.1:n.1857-82G>A
(GMPPA)
|
|
|
|
ENST00000683626.1:c.*1460G>A
(GMPPA)
|
ENSP00000507216.1:n.*1460G>A
|
|
|
ENST00000683691.1:c.*707G>A
(GMPPA)
|
ENSP00000508392.1:n.*707G>A
|
|
|
ENST00000683746.1:n.1766G>A
(GMPPA)
|
|
|
|
ENST00000683752.1:c.465G>A
(GMPPA)
|
ENSP00000507197.1:p.Arg155=
|
|
|
ENST00000683864.1:c.*1596G>A
(GMPPA)
|
ENSP00000507147.1:n.*1596G>A
|
|
|
ENST00000683946.1:c.816G>A
(GMPPA)
|
ENSP00000506941.1:p.Arg272=
|
|
|
ENST00000684227.1:c.*847G>A
(GMPPA)
|
ENSP00000507190.1:n.*847G>A
|
|
|
ENST00000684242.1:n.1794-82G>A
(GMPPA)
|
|
|
|
ENST00000684274.1:n.1186G>A
(GMPPA)
|
|
|
|
ENST00000684334.1:n.1901G>A
(GMPPA)
|
|
|
|
ENST00000684412.1:n.1162G>A
(GMPPA)
|
|
|
|
ENST00000684562.1:n.1836G>A
(GMPPA)
|
|
|
|
ENST00000684706.1:n.880G>A
(GMPPA)
|
|
|
|
ENST00000684729.1:c.*847G>A
(GMPPA)
|
ENSP00000507441.1:n.*847G>A
|
|
|
ENST00000313597.10:c.816G>A
(GMPPA)
MANE Select
|
ENSP00000315925.6:p.Arg272=
|
|
|
ENST00000313597.9:c.816G>A
(GMPPA)
|
ENSP00000315925.5:p.Arg272=
|
|
|
ENST00000341142.7:c.816G>A
(GMPPA)
|
ENSP00000340760.3:p.Arg272=
|
|
|
ENST00000358215.8:c.816G>A
(GMPPA)
|
ENSP00000350949.3:p.Arg272=
|
|
|
ENST00000373908.5:c.816G>A
(GMPPA)
|
ENSP00000363016.1:p.Arg272=
|
|
|
ENST00000373917.7:c.816G>A
(GMPPA)
|
ENSP00000363027.3:p.Arg272=
|
|
|
ENST00000435316.5:c.711G>A
(GMPPA)
|
ENSP00000411060.1:p.Arg237=
|
|
|
ENST00000443704.5:c.816G>A
(GMPPA)
|
ENSP00000396750.1:p.Arg272=
|
|
|
ENST00000481170.1:n.3654G>A
(GMPPA)
|
|
|
|
ENST00000622191.1:c.816G>A
(GMPPA)
|
ENSP00000478700.1:p.Arg272=
|
|
|
NM_013335.3:c.816G>A
(GMPPA)
|
NP_037467.2:p.Arg272=
|
|
|
NM_205847.2:c.816G>A
(GMPPA)
|
NP_995319.1:p.Arg272=
|
|
|
XM_005246483.2:c.831G>A
(GMPPA)
|
XP_005246540.1:p.Arg277=
|
|
|
XM_005246485.2:c.831G>A
(GMPPA)
|
XP_005246542.1:p.Arg277=
|
|
|
XM_005246486.2:c.816G>A
(GMPPA)
|
XP_005246543.1:p.Arg272=
|
|
|
XM_011511032.1:c.831G>A
(GMPPA)
|
XP_011509334.1:p.Arg277=
|
|
|
XM_011511033.1:c.456G>A
(GMPPA)
|
XP_011509335.1:p.Arg152=
|
|
|
XM_011511034.1:c.831G>A
(GMPPA)
|
XP_011509336.1:p.Arg277=
|
|
|
XM_011511035.1:c.771-82G>A
(GMPPA)
|
XP_011509337.1:n.771-82G>A
|
|
|
XR_241307.2:n.910G>A
(GMPPA)
|
|
|
|
XR_923921.1:n.352+11178C>T
(ASIC4-AS1)
|
|
|
|
XM_005246486.3:c.816G>A
(GMPPA)
|
XP_005246543.1:p.Arg272=
|
|
|
XM_024452823.1:c.816G>A
(GMPPA)
|
XP_024308591.1:p.Arg272=
|
|
|
XR_923921.2:n.391+11178C>T
(ASIC4-AS1)
|
|
|
|
NM_001374294.1:c.816G>A
(GMPPA)
|
NP_001361223.1:p.Arg272=
|
|
|
NM_001374295.1:c.816G>A
(GMPPA)
|
NP_001361224.1:p.Arg272=
|
|
|
NM_013335.4:c.816G>A
(GMPPA)
MANE Select
|
NP_037467.2:p.Arg272=
|
|
|
NM_205847.3:c.816G>A
(GMPPA)
|
NP_995319.1:p.Arg272=
|
|
