ENST00000295897.9:c.1132G=
MANE Select
|
ENSP00000295897.4:p.Glu378=
|
|
ENST00000295897.8:c.1132G=
|
ENSP00000295897.4:p.Glu378=
|
|
ENST00000401494.7:c.787G=
|
ENSP00000384695.3:p.Glu263=
|
|
ENST00000415165.6:c.556G=
|
ENSP00000401820.2:p.Glu186=
|
|
ENST00000476441.6:c.*411G=
|
ENSP00000423727.1:n.*411G=
|
|
ENST00000484992.1:n.452G=
|
|
|
ENST00000503124.5:c.682G=
|
ENSP00000421027.1:p.Glu228=
|
|
ENST00000504043.1:n.135G=
|
|
|
ENST00000505649.5:n.818G=
|
|
|
ENST00000509063.5:c.1132G=
|
ENSP00000422784.1:p.Glu378=
|
|
ENST00000511370.1:c.665G=
|
|
|
ENST00000621085.4:c.493G=
|
ENSP00000483421.1:p.Glu165=
|
|
ENST00000621628.4:c.493G=
|
ENSP00000480485.1:p.Glu165=
|
|
NM_000477.5:c.1132G=
|
NP_000468.1:p.Glu378=
|
|
NM_000477.6:c.1132G=
|
NP_000468.1:p.Glu378=
|
|
NM_000477.7:c.1132G=
MANE Select
|
NP_000468.1:p.Glu378=
|
|