ENST00000396705.10:c.702T>A
MANE Select
|
ENSP00000379933.4:p.Gly234=
|
|
ENST00000229270.8:c.813T>A
|
ENSP00000229270.4:p.Gly271=
|
|
ENST00000396705.9:c.702T>A
|
ENSP00000379933.4:p.Gly234=
|
|
ENST00000474253.1:n.191T>A
|
|
|
ENST00000488464.6:c.456T>A
|
ENSP00000475620.1:p.Gly152=
|
|
ENST00000535434.5:c.456T>A
|
ENSP00000443599.1:p.Gly152=
|
|
ENST00000613953.4:c.813T>A
|
ENSP00000484435.1:p.Gly271=
|
|
NM_000365.5:c.702T>A
|
NP_000356.1:p.Gly234=
|
|
NM_001159287.1:c.813T>A
|
NP_001152759.1:p.Gly271=
|
|
NM_001258026.1:c.456T>A
|
NP_001244955.1:p.Gly152=
|
|
XR_002957378.1:n.1710T>A
|
|
|
NM_000365.6:c.702T>A
MANE Select
|
NP_000356.1:p.Gly234=
|
|
NM_001258026.2:c.456T>A
|
NP_001244955.1:p.Gly152=
|
|