ENST00000695901.1:c.798+774C>T
|
ENSP00000512251.1:n.798+774C>T
|
|
ENST00000695911.1:c.897C>T
|
ENSP00000512262.1:n.897C>T
|
|
ENST00000695912.1:c.1116C>T
|
ENSP00000512263.1:p.Gly372=
|
|
ENST00000695913.1:c.*1872C>T
|
ENSP00000512264.1:n.*1872C>T
|
|
ENST00000695914.1:c.879C>T
|
ENSP00000512265.1:p.Gly293=
|
|
ENST00000695918.1:n.347C>T
|
|
|
ENST00000306721.8:c.1119C>T
MANE Select
|
ENSP00000306968.3:p.Gly373=
|
|
ENST00000306721.7:c.1119C>T
|
ENSP00000306968.3:p.Gly373=
|
|
ENST00000347703.7:c.882C>T
|
ENSP00000272789.4:p.Gly294=
|
|
ENST00000410019.3:c.756C>T
|
ENSP00000386833.3:p.Gly252=
|
|
ENST00000410101.7:c.987C>T
|
ENSP00000386656.3:p.Gly329=
|
|
ENST00000467411.5:n.1768+774C>T
|
|
|
ENST00000496441.5:n.1873C>T
|
|
|
NM_031942.4:c.1119C>T
|
NP_114148.3:p.Gly373=
|
|
NM_145810.2:c.882C>T
|
NP_665809.1:p.Gly294=
|
|
XM_011511957.1:c.1038C>T
|
XP_011510259.1:p.Gly346=
|
|
XR_923034.1:n.2017C>T
|
|
|
NM_031942.5:c.1119C>T
MANE Select
|
NP_114148.3:p.Gly373=
|
|
NM_145810.3:c.882C>T
|
NP_665809.1:p.Gly294=
|
|