ENST00000225573.5:c.602G>T
|
ENSP00000225573.5:p.Gly201Val
|
|
ENST00000434554.7:c.677G>T
|
ENSP00000399960.3:p.Gly226Val
|
|
ENST00000582171.6:c.*396G>T
|
ENSP00000463994.1:n.*396G>T
|
|
ENST00000583599.6:c.491G>T
|
ENSP00000463919.2:p.Gly164Val
|
|
ENST00000584061.6:c.662G>T
|
ENSP00000463972.2:p.Gly221Val
|
|
ENST00000584806.2:n.400G>T
|
|
|
ENST00000641305.1:n.2230G>T
|
|
|
ENST00000641323.1:c.*750G>T
|
ENSP00000492965.1:n.*750G>T
|
|
ENST00000641427.1:n.731G>T
|
|
|
ENST00000641703.1:c.447G>T
|
ENSP00000493219.1:n.447G>T
|
|
ENST00000641709.1:c.*553G>T
|
ENSP00000493349.1:n.*553G>T
|
|
ENST00000641856.1:c.*1239G>T
|
ENSP00000493224.1:n.*1239G>T
|
|
ENST00000642017.2:c.731G>T
MANE Select
|
ENSP00000493302.2:p.Gly244Val
|
|
ENST00000225573.4:c.731G>T
|
ENSP00000225573.4:p.Gly244Val
|
|
ENST00000434554.6:c.602G>T
|
ENSP00000399960.2:p.Gly201Val
|
|
ENST00000582171.5:c.*396G>T
|
ENSP00000463994.1:n.*396G>T
|
|
ENST00000584806.1:n.400G>T
|
|
|
ENST00000585320.5:c.*213G>T
|
ENSP00000462345.1:n.*213G>T
|
|
NM_018129.3:c.731G>T
|
NP_060599.1:p.Gly244Val
|
|
XM_005257500.2:c.491G>T
|
XP_005257557.1:p.Gly164Val
|
|
XM_011524968.1:c.446G>T
|
XP_011523270.1:p.Gly149Val
|
|
XM_005257500.3:c.491G>T
|
XP_005257557.1:p.Gly164Val
|
|
XM_011524968.2:c.446G>T
|
XP_011523270.1:p.Gly149Val
|
|
XM_017024813.1:c.491G>T
|
XP_016880302.1:p.Gly164Val
|
|
NM_018129.4:c.731G>T
MANE Select
|
NP_060599.1:p.Gly244Val
|
|