ENST00000225573.5:c.587G>A
|
ENSP00000225573.5:p.Gly196Glu
|
|
ENST00000434554.7:c.662G>A
|
ENSP00000399960.3:p.Gly221Glu
|
|
ENST00000582171.6:c.*381G>A
|
ENSP00000463994.1:n.*381G>A
|
|
ENST00000583599.6:c.476G>A
|
ENSP00000463919.2:p.Gly159Glu
|
|
ENST00000584061.6:c.647G>A
|
ENSP00000463972.2:p.Gly216Glu
|
|
ENST00000584806.2:n.385G>A
|
|
|
ENST00000641305.1:n.2215G>A
|
|
|
ENST00000641323.1:c.*735G>A
|
ENSP00000492965.1:n.*735G>A
|
|
ENST00000641427.1:n.716G>A
|
|
|
ENST00000641511.1:c.448G>A
|
|
|
ENST00000641703.1:c.432G>A
|
ENSP00000493219.1:n.432G>A
|
|
ENST00000641709.1:c.*538G>A
|
ENSP00000493349.1:n.*538G>A
|
|
ENST00000641856.1:c.*1224G>A
|
ENSP00000493224.1:n.*1224G>A
|
|
ENST00000642017.2:c.716G>A
MANE Select
|
ENSP00000493302.2:p.Gly239Glu
|
|
ENST00000225573.4:c.716G>A
|
ENSP00000225573.4:p.Gly239Glu
|
|
ENST00000434554.6:c.587G>A
|
ENSP00000399960.2:p.Gly196Glu
|
|
ENST00000582171.5:c.*381G>A
|
ENSP00000463994.1:n.*381G>A
|
|
ENST00000584806.1:n.385G>A
|
|
|
ENST00000585320.5:c.*198G>A
|
ENSP00000462345.1:n.*198G>A
|
|
NM_018129.3:c.716G>A
|
NP_060599.1:p.Gly239Glu
|
|
XM_005257500.2:c.476G>A
|
XP_005257557.1:p.Gly159Glu
|
|
XM_011524968.1:c.431G>A
|
XP_011523270.1:p.Gly144Glu
|
|
XM_005257500.3:c.476G>A
|
XP_005257557.1:p.Gly159Glu
|
|
XM_011524968.2:c.431G>A
|
XP_011523270.1:p.Gly144Glu
|
|
XM_017024813.1:c.476G>A
|
XP_016880302.1:p.Gly159Glu
|
|
NM_018129.4:c.716G>A
MANE Select
|
NP_060599.1:p.Gly239Glu
|
|