ENST00000527168.6:n.741G=
|
|
|
ENST00000529110.2:c.726G=
|
ENSP00000435349.2:p.Glu242=
|
|
ENST00000529957.6:n.700G=
|
|
|
ENST00000683366.1:c.*374G=
|
ENSP00000507283.1:n.*374G=
|
|
ENST00000683887.1:c.690G=
|
ENSP00000506886.1:p.Glu230=
|
|
ENST00000684100.1:n.636G=
|
|
|
ENST00000684126.1:n.776G=
|
|
|
ENST00000684688.1:n.1267G=
|
|
|
ENST00000204679.9:c.642G=
MANE Select
|
ENSP00000204679.4:p.Glu214=
|
|
ENST00000204679.8:c.642G=
|
ENSP00000204679.4:p.Glu214=
|
|
ENST00000527076.1:n.1865G=
|
|
|
ENST00000527168.5:n.809G=
|
|
|
ENST00000529957.5:n.741G=
|
|
|
NM_032520.4:c.642G=
|
NP_115909.1:p.Glu214=
|
|
XM_017023782.1:c.690G=
|
XP_016879271.1:p.Glu230=
|
|
XM_017023783.1:c.282G=
|
XP_016879272.1:p.Glu94=
|
|
NM_032520.5:c.642G=
MANE Select
|
NP_115909.1:p.Glu214=
|
|