ENST00000682424.1:c.774C>T
|
ENSP00000507321.1:p.Gly258=
|
|
ENST00000299427.12:c.888C>T
MANE Select
|
ENSP00000299427.6:p.Gly296=
|
|
ENST00000436873.7:c.313-428C>T
|
|
|
ENST00000530040.2:n.481C>T
|
|
|
ENST00000533371.6:c.159C>T
|
ENSP00000437066.1:p.Gly53=
|
|
ENST00000642892.1:c.159C>T
|
ENSP00000494165.1:p.Gly53=
|
|
ENST00000643439.1:c.*628C>T
|
ENSP00000495849.1:n.*628C>T
|
|
ENST00000643479.1:n.1074C>T
|
|
|
ENST00000643516.1:c.397C>T
|
|
|
ENST00000644218.1:c.886+159C>T
|
ENSP00000493574.1:n.886+159C>T
|
|
ENST00000644683.1:c.*341C>T
|
ENSP00000494085.1:n.*341C>T
|
|
ENST00000644810.1:c.609C>T
|
ENSP00000495895.1:p.Gly203=
|
|
ENST00000644831.1:n.1064C>T
|
|
|
ENST00000644933.1:c.159C>T
|
ENSP00000496133.1:p.Gly53=
|
|
ENST00000645285.1:c.157+159C>T
|
ENSP00000495058.1:n.157+159C>T
|
|
ENST00000645331.1:n.1411C>T
|
|
|
ENST00000645620.1:c.159C>T
|
ENSP00000493657.1:p.Gly53=
|
|
ENST00000646777.1:n.1221C>T
|
|
|
ENST00000647016.1:n.1368C>T
|
|
|
ENST00000647152.1:c.159C>T
|
ENSP00000495893.1:p.Gly53=
|
|
ENST00000647209.1:c.*757C>T
|
ENSP00000495558.1:n.*757C>T
|
|
ENST00000647346.1:n.1908C>T
|
|
|
ENST00000299427.10:c.888C>T
|
ENSP00000299427.6:p.Gly296=
|
|
ENST00000436873.6:c.452C>T
|
ENSP00000398136.2:p.Ala151Val
|
|
ENST00000533371.5:c.159C>T
|
ENSP00000437066.1:p.Gly53=
|
|
ENST00000611494.4:c.888C>T
|
ENSP00000484546.1:p.Gly296=
|
|
NM_000391.3:c.888C>T
|
NP_000382.3:p.Gly296=
|
|
NM_000391.4:c.888C>T
MANE Select
|
NP_000382.3:p.Gly296=
|
|