|
NM_001199138.2:c.2714A>G
MANE Select
|
NP_001186067.1:p.Glu905Gly
|
|
ENST00000402280.6:c.2714A>G
MANE Select
|
ENSP00000385428.1:p.Glu905Gly
|
|
NM_001199138.1:c.2714A>G
|
NP_001186067.1:p.Glu905Gly
|
|
NM_001199139.1:c.2714A>G
|
NP_001186068.1:p.Glu905Gly
|
|
NM_001302504.1:c.719A>G
|
NP_001289433.1:p.Glu240Gly
|
|
NM_021209.4:c.2714A>G
|
NP_067032.3:p.Glu905Gly
|
|
ENST00000342905.10:c.719A>G
|
ENSP00000339666.6:p.Glu240Gly
|
|
ENST00000360906.9:c.2714A>G
|
ENSP00000354159.5:p.Glu905Gly
|
|
ENST00000402280.5:c.2714A>G
|
ENSP00000385428.1:p.Glu905Gly
|
|
ENST00000404025.2:c.2714A>G
|
ENSP00000385090.2:p.Glu905Gly
|
|
ENST00000404025.3:c.*420A>G
|
ENSP00000385090.3:n.*420A>G
|
|
ENST00000652197.1:c.*444A>G
|
ENSP00000498301.1:n.*444A>G
|
|
ENST00000652197.2:c.407A>G
|
ENSP00000498301.2:p.Glu136Gly
|
|
XR_001738872.1:n.2980A>G
|
|