ENST00000281543.6:c.1613+159G>T
(GUF1)
MANE Select
|
ENSP00000281543.5:n.1613+159G>T
|
|
ENST00000281543.5:c.1613+159G>T
(GUF1)
|
ENSP00000281543.5:n.1613+159G>T
|
|
ENST00000506793.5:n.1495+159G>T
(GUF1)
|
|
|
ENST00000608855.1:c.128-9316C>A
(GNPDA2)
|
ENSP00000477137.1:n.128-9316C>A
|
|
ENST00000609092.5:c.247-9316C>A
(GNPDA2)
|
|
|
NM_021927.2:c.1613+159G>T
(GUF1)
|
NP_068746.2:n.1613+159G>T
|
|
XM_005248122.2:c.641+159G>T
(GUF1)
|
XP_005248179.1:n.641+159G>T
|
|
XM_011513625.1:c.770-9316C>A
(GNPDA2)
|
XP_011511927.1:n.770-9316C>A
|
|
XM_011513626.1:c.560-9316C>A
(GNPDA2)
|
XP_011511928.1:n.560-9316C>A
|
|
XM_011513732.1:c.1613+159G>T
(GUF1)
|
XP_011512034.1:n.1613+159G>T
|
|
XM_011513733.1:c.1463+159G>T
(GUF1)
|
XP_011512035.1:n.1463+159G>T
|
|
XM_011513734.1:c.1479+1098G>T
(GUF1)
|
XP_011512036.1:n.1479+1098G>T
|
|
NM_001345867.1:c.641+159G>T
(GUF1)
|
NP_001332796.1:n.641+159G>T
|
|
NM_001345868.1:c.1613+159G>T
(GUF1)
|
NP_001332797.1:n.1613+159G>T
|
|
NM_001345869.1:c.641+159G>T
(GUF1)
|
NP_001332798.1:n.641+159G>T
|
|
XM_024454178.1:c.1463+159G>T
(GUF1)
|
XP_024309946.1:n.1463+159G>T
|
|
NM_021927.3:c.1613+159G>T
(GUF1)
MANE Select
|
NP_068746.2:n.1613+159G>T
|
|
NM_001345867.2:c.641+159G>T
(GUF1)
|
NP_001332796.1:n.641+159G>T
|
|
NM_001345868.2:c.1613+159G>T
(GUF1)
|
NP_001332797.1:n.1613+159G>T
|
|
NM_001345869.2:c.641+159G>T
(GUF1)
|
NP_001332798.1:n.641+159G>T
|
|