ENST00000527168.6:n.880G>T
|
|
|
ENST00000529110.2:c.865G>T
|
ENSP00000435349.2:p.Gly289Cys
|
|
ENST00000529957.6:n.839G>T
|
|
|
ENST00000683366.1:c.*513G>T
|
ENSP00000507283.1:n.*513G>T
|
|
ENST00000683887.1:c.829G>T
|
ENSP00000506886.1:p.Gly277Cys
|
|
ENST00000684100.1:n.775G>T
|
|
|
ENST00000684126.1:n.915G>T
|
|
|
ENST00000684688.1:n.1406G>T
|
|
|
ENST00000204679.9:c.781G>T
MANE Select
|
ENSP00000204679.4:p.Gly261Cys
|
|
ENST00000204679.8:c.781G>T
|
ENSP00000204679.4:p.Gly261Cys
|
|
ENST00000527076.1:n.2004G>T
|
|
|
ENST00000527168.5:n.948G>T
|
|
|
ENST00000529957.5:n.880G>T
|
|
|
NM_032520.4:c.781G>T
|
NP_115909.1:p.Gly261Cys
|
|
XM_017023782.1:c.829G>T
|
XP_016879271.1:p.Gly277Cys
|
|
XM_017023783.1:c.421G>T
|
XP_016879272.1:p.Gly141Cys
|
|
NM_032520.5:c.781G>T
MANE Select
|
NP_115909.1:p.Gly261Cys
|
|