ENST00000225573.5:c.575G>T
|
ENSP00000225573.5:p.Gly192Val
|
|
ENST00000434554.7:c.650G>T
|
ENSP00000399960.3:p.Gly217Val
|
|
ENST00000582171.6:c.*369G>T
|
ENSP00000463994.1:n.*369G>T
|
|
ENST00000583599.6:c.464G>T
|
ENSP00000463919.2:p.Gly155Val
|
|
ENST00000584061.6:c.635G>T
|
ENSP00000463972.2:p.Gly212Val
|
|
ENST00000584806.2:n.373G>T
|
|
|
ENST00000641285.1:n.484G>T
|
|
|
ENST00000641305.1:n.2203G>T
|
|
|
ENST00000641323.1:c.*723G>T
|
ENSP00000492965.1:n.*723G>T
|
|
ENST00000641427.1:n.704G>T
|
|
|
ENST00000641511.1:c.436G>T
|
|
|
ENST00000641703.1:c.420G>T
|
ENSP00000493219.1:n.420G>T
|
|
ENST00000641709.1:c.*526G>T
|
ENSP00000493349.1:n.*526G>T
|
|
ENST00000641856.1:c.*1212G>T
|
ENSP00000493224.1:n.*1212G>T
|
|
ENST00000642017.2:c.704G>T
MANE Select
|
ENSP00000493302.2:p.Gly235Val
|
|
ENST00000225573.4:c.704G>T
|
ENSP00000225573.4:p.Gly235Val
|
|
ENST00000434554.6:c.575G>T
|
ENSP00000399960.2:p.Gly192Val
|
|
ENST00000582171.5:c.*369G>T
|
ENSP00000463994.1:n.*369G>T
|
|
ENST00000584806.1:n.373G>T
|
|
|
ENST00000585320.5:c.*186G>T
|
ENSP00000462345.1:n.*186G>T
|
|
NM_018129.3:c.704G>T
|
NP_060599.1:p.Gly235Val
|
|
XM_005257500.2:c.464G>T
|
XP_005257557.1:p.Gly155Val
|
|
XM_011524968.1:c.419G>T
|
XP_011523270.1:p.Gly140Val
|
|
XM_005257500.3:c.464G>T
|
XP_005257557.1:p.Gly155Val
|
|
XM_011524968.2:c.419G>T
|
XP_011523270.1:p.Gly140Val
|
|
XM_017024813.1:c.464G>T
|
XP_016880302.1:p.Gly155Val
|
|
NM_018129.4:c.704G>T
MANE Select
|
NP_060599.1:p.Gly235Val
|
|