ENST00000570382.2:c.981C>T
|
ENSP00000466346.2:p.Ile327=
|
|
ENST00000571691.6:c.909C>T
|
ENSP00000461407.2:p.Ile303=
|
|
ENST00000571721.6:c.981C>T
|
ENSP00000460660.2:p.Ile327=
|
|
ENST00000572105.7:c.*425C>T
|
ENSP00000462823.1:n.*425C>T
|
|
ENST00000573283.7:c.981C>T
MANE Select
|
ENSP00000458435.1:p.Ile327=
|
|
ENST00000574671.6:n.1381C>T
|
|
|
ENST00000575659.6:c.981C>T
|
ENSP00000459119.2:p.Ile327=
|
|
ENST00000575994.6:c.981C>T
|
ENSP00000460464.2:p.Ile327=
|
|
ENST00000576214.3:n.1282C>T
|
|
|
ENST00000576544.6:c.981C>T
|
ENSP00000461672.1:p.Ile327=
|
|
ENST00000615544.5:c.981C>T
|
ENSP00000477968.1:p.Ile327=
|
|
ENST00000644774.2:c.954C>T
|
ENSP00000493648.2:p.Ile318=
|
|
ENST00000679410.1:n.1184C>T
|
|
|
ENST00000679480.1:c.981C>T
|
ENSP00000506201.1:p.Ile327=
|
|
ENST00000679535.1:n.1282C>T
|
|
|
ENST00000679778.1:c.981C>T
|
ENSP00000505235.1:p.Ile327=
|
|
ENST00000680227.1:c.981C>T
|
ENSP00000506253.1:p.Ile327=
|
|
ENST00000680727.1:c.981C>T
|
ENSP00000505193.1:p.Ile327=
|
|
ENST00000681052.1:c.981C>T
|
ENSP00000505060.1:p.Ile327=
|
|
ENST00000681092.1:c.*785C>T
|
ENSP00000506720.1:n.*785C>T
|
|
ENST00000681842.1:c.981C>T
|
ENSP00000506126.1:p.Ile327=
|
|
ENST00000331925.6:c.981C>T
|
ENSP00000331514.2:p.Ile327=
|
|
ENST00000572105.6:c.*425C>T
|
ENSP00000462823.1:n.*425C>T
|
|
ENST00000573283.5:c.981C>T
|
ENSP00000458435.1:p.Ile327=
|
|
ENST00000574671.5:n.840C>T
|
|
|
ENST00000575087.5:c.981C>T
|
ENSP00000459124.1:p.Ile327=
|
|
ENST00000575842.5:c.981C>T
|
ENSP00000458162.1:p.Ile327=
|
|
ENST00000576209.5:n.866C>T
|
|
|
ENST00000576544.5:c.981C>T
|
ENSP00000461672.1:p.Ile327=
|
|
ENST00000576917.5:n.1113C>T
|
|
|
ENST00000615544.4:c.981C>T
|
ENSP00000477968.1:p.Ile327=
|
|
NM_001199954.1:c.981C>T
|
NP_001186883.1:p.Ile327=
|
|
NM_001614.3:c.981C>T
|
NP_001605.1:p.Ile327=
|
|
NR_037688.1:n.1120C>T
|
|
|
NM_001199954.2:c.981C>T
|
NP_001186883.1:p.Ile327=
|
|
NM_001614.4:c.981C>T
|
NP_001605.1:p.Ile327=
|
|
NR_037688.2:n.1053C>T
|
|
|
NM_001614.5:c.981C>T
MANE Select
|
NP_001605.1:p.Ile327=
|
|
NR_037688.3:n.1053C>T
|
|
|
NM_001199954.3:c.981C>T
|
NP_001186883.1:p.Ile327=
|
|