ENST00000527168.6:n.881G>A
|
|
|
ENST00000529110.2:c.866G>A
|
ENSP00000435349.2:p.Gly289Asp
|
|
ENST00000529957.6:n.840G>A
|
|
|
ENST00000683366.1:c.*514G>A
|
ENSP00000507283.1:n.*514G>A
|
|
ENST00000683887.1:c.830G>A
|
ENSP00000506886.1:p.Gly277Asp
|
|
ENST00000684100.1:n.776G>A
|
|
|
ENST00000684126.1:n.916G>A
|
|
|
ENST00000684688.1:n.1407G>A
|
|
|
ENST00000204679.9:c.782G>A
MANE Select
|
ENSP00000204679.4:p.Gly261Asp
|
|
ENST00000204679.8:c.782G>A
|
ENSP00000204679.4:p.Gly261Asp
|
|
ENST00000527076.1:n.2005G>A
|
|
|
ENST00000527168.5:n.949G>A
|
|
|
ENST00000529957.5:n.881G>A
|
|
|
NM_032520.4:c.782G>A
|
NP_115909.1:p.Gly261Asp
|
|
XM_017023782.1:c.830G>A
|
XP_016879271.1:p.Gly277Asp
|
|
XM_017023783.1:c.422G>A
|
XP_016879272.1:p.Gly141Asp
|
|
NM_032520.5:c.782G>A
MANE Select
|
NP_115909.1:p.Gly261Asp
|
|