ENST00000527168.6:n.885G=
|
|
|
ENST00000529110.2:c.870G=
|
ENSP00000435349.2:p.Leu290=
|
|
ENST00000529957.6:n.844G=
|
|
|
ENST00000683366.1:c.*518G=
|
ENSP00000507283.1:n.*518G=
|
|
ENST00000683887.1:c.834G=
|
ENSP00000506886.1:p.Leu278=
|
|
ENST00000684100.1:n.780G=
|
|
|
ENST00000684126.1:n.920G=
|
|
|
ENST00000684688.1:n.1411G=
|
|
|
ENST00000204679.9:c.786G=
MANE Select
|
ENSP00000204679.4:p.Leu262=
|
|
ENST00000204679.8:c.786G=
|
ENSP00000204679.4:p.Leu262=
|
|
ENST00000527076.1:n.2009G=
|
|
|
ENST00000527168.5:n.953G=
|
|
|
ENST00000529957.5:n.885G=
|
|
|
NM_032520.4:c.786G=
|
NP_115909.1:p.Leu262=
|
|
XM_017023782.1:c.834G=
|
XP_016879271.1:p.Leu278=
|
|
XM_017023783.1:c.426G=
|
XP_016879272.1:p.Leu142=
|
|
NM_032520.5:c.786G=
MANE Select
|
NP_115909.1:p.Leu262=
|
|