ENST00000548747.6:c.906C>A
MANE Select
|
ENSP00000448828.1:p.Gly302=
|
|
ENST00000449260.6:c.906C>A
|
ENSP00000402758.2:p.Gly302=
|
|
ENST00000546543.5:c.759C>A
|
ENSP00000446662.1:p.Gly253=
|
|
ENST00000547137.5:c.744C>A
|
ENSP00000448849.1:p.Gly248=
|
|
ENST00000548493.5:c.906C>A
|
ENSP00000447374.1:p.Gly302=
|
|
ENST00000548747.5:c.906C>A
|
ENSP00000448828.1:p.Gly302=
|
|
ENST00000548803.5:c.470-11C>A
|
ENSP00000447732.1:n.470-11C>A
|
|
ENST00000549404.5:c.568C>A
|
|
|
ENST00000550447.5:c.358+1076C>A
|
ENSP00000448029.1:n.358+1076C>A
|
|
ENST00000550464.5:c.648C>A
|
ENSP00000450036.1:p.Gly216=
|
|
ENST00000552882.5:c.906C>A
|
ENSP00000449690.1:p.Gly302=
|
|
ENST00000556802.1:n.642C>A
|
|
|
NM_001200053.1:c.648C>A
|
NP_001186982.1:p.Gly216=
|
|
NM_001200054.1:c.906C>A
|
NP_001186983.1:p.Gly302=
|
|
NM_006928.4:c.906C>A
|
NP_008859.1:p.Gly302=
|
|
XM_006719569.1:c.906C>A
|
XP_006719632.1:p.Gly302=
|
|
XM_011538685.1:c.906C>A
|
XP_011536987.1:p.Gly302=
|
|
XM_011538686.1:c.906C>A
|
XP_011536988.1:p.Gly302=
|
|
XM_011538687.1:c.906C>A
|
XP_011536989.1:p.Gly302=
|
|
NM_001320121.1:c.906C>A
|
NP_001307050.1:p.Gly302=
|
|
NM_001320122.1:c.906C>A
|
NP_001307051.1:p.Gly302=
|
|
NM_001384361.1:c.906C>A
MANE Select
|
NP_001371290.1:p.Gly302=
|
|
NM_006928.5:c.906C>A
|
NP_008859.1:p.Gly302=
|
|