|
ENST00000396594.8:c.2005G>T
(GNE)
MANE Plus Clinical
|
ENSP00000379839.3:p.Ala669Ser
|
|
|
ENST00000543356.7:c.1735G>T
(GNE)
|
ENSP00000437765.3:p.Ala579Ser
|
|
|
ENST00000642385.2:c.1912G>T
(GNE)
MANE Select
|
ENSP00000494141.2:p.Ala638Ser
|
|
|
ENST00000377902.5:c.1912G>T
(GNE)
|
ENSP00000367134.4:p.Ala638Ser
|
|
|
ENST00000396594.7:c.2005G>T
(GNE)
|
ENSP00000379839.3:p.Ala669Ser
|
|
|
ENST00000447283.6:c.1690G>T
(GNE)
|
ENSP00000414760.2:p.Ala564Ser
|
|
|
ENST00000464497.5:c.485+14025C>A
(CLTA)
|
ENSP00000419158.1:n.485+14025C>A
|
|
|
ENST00000539208.5:c.1582G>T
(GNE)
|
ENSP00000445117.1:p.Ala528Ser
|
|
|
ENST00000539815.5:c.1912G>T
(GNE)
|
ENSP00000439155.1:p.Ala638Ser
|
|
|
ENST00000543356.6:c.1897G>T
(GNE)
|
ENSP00000437765.2:p.Ala633Ser
|
|
|
NM_001128227.2:c.2005G>T
(GNE)
|
NP_001121699.1:p.Ala669Ser
|
|
|
NM_001190383.1:c.1690G>T
(GNE)
|
NP_001177312.1:p.Ala564Ser
|
|
|
NM_001190384.1:c.1582G>T
(GNE)
|
NP_001177313.1:p.Ala528Ser
|
|
|
NM_001190388.1:c.1897G>T
(GNE)
|
NP_001177317.1:p.Ala633Ser
|
|
|
NM_005476.5:c.1912G>T
(GNE)
|
NP_005467.1:p.Ala638Ser
|
|
|
XM_005251334.3:c.1852G>T
(GNE)
|
XP_005251391.1:p.Ala618Ser
|
|
|
NM_001190383.2:c.1690G>T
(GNE)
|
NP_001177312.1:p.Ala564Ser
|
|
|
NM_001190384.2:c.1582G>T
(GNE)
|
NP_001177313.1:p.Ala528Ser
|
|
|
NM_005476.6:c.1912G>T
(GNE)
|
NP_005467.1:p.Ala638Ser
|
|
|
XM_005251334.4:c.1852G>T
(GNE)
|
XP_005251391.1:p.Ala618Ser
|
|
|
XM_017014167.1:c.1912G>T
(GNE)
|
XP_016869656.1:p.Ala638Ser
|
|
|
XM_017014168.1:c.1759G>T
(GNE)
|
XP_016869657.1:p.Ala587Ser
|
|
|
NM_001128227.3:c.2005G>T
(GNE)
MANE Plus Clinical
|
NP_001121699.1:p.Ala669Ser
|
|
|
NM_001190383.3:c.1690G>T
(GNE)
|
NP_001177312.1:p.Ala564Ser
|
|
|
NM_001190384.3:c.1582G>T
(GNE)
|
NP_001177313.1:p.Ala528Ser
|
|
|
NM_001190388.2:c.1735G>T
(GNE)
|
NP_001177317.2:p.Ala579Ser
|
|
|
NM_001374797.1:c.1759G>T
(GNE)
|
NP_001361726.1:p.Ala587Ser
|
|
|
NM_001374798.1:c.1735G>T
(GNE)
|
NP_001361727.1:p.Ala579Ser
|
|
|
NM_005476.7:c.1912G>T
(GNE)
MANE Select
|
NP_005467.1:p.Ala638Ser
|
|
