ENST00000391944.8:c.1758G>A
|
ENSP00000375808.4:p.Glu586=
|
|
ENST00000682414.1:c.1758G>A
|
ENSP00000507019.1:p.Glu586=
|
|
ENST00000682508.1:n.1787G>A
|
|
|
ENST00000684218.1:c.*1016G>A
|
ENSP00000507804.1:n.*1016G>A
|
|
ENST00000684264.1:n.1314G>A
|
|
|
ENST00000684407.1:c.1635G>A
|
ENSP00000507775.1:p.Glu545=
|
|
ENST00000684458.1:c.*244G>A
|
ENSP00000508260.1:n.*244G>A
|
|
ENST00000684468.1:n.1470G>A
|
|
|
ENST00000391945.10:c.1758G>A
MANE Select
|
ENSP00000375809.4:p.Glu586=
|
|
ENST00000587376.6:c.817G>A
|
|
|
ENST00000646507.1:n.1855G>A
|
|
|
ENST00000391941.6:c.1686G>A
|
ENSP00000375805.2:p.Glu562=
|
|
ENST00000391942.6:n.929G>A
|
|
|
ENST00000391944.7:c.1524G>A
|
ENSP00000375808.3:p.Glu508=
|
|
ENST00000391945.8:c.1758G>A
|
ENSP00000375809.3:p.Glu586=
|
|
ENST00000587376.5:c.817G>A
|
|
|
ENST00000588652.5:n.1846G>A
|
|
|
NM_000400.3:c.1758G>A , LRG_461t1:c.1758G>A
|
NP_000391.1:p.Glu586=
|
|
XM_011526611.1:c.1680G>A
|
XP_011524913.1:p.Glu560=
|
|
XR_935763.1:n.1741G>A
|
|
|
XM_011526611.2:c.1680G>A
|
XP_011524913.1:p.Glu560=
|
|
XM_017026467.1:c.1635G>A
|
XP_016881956.1:p.Glu545=
|
|
XR_001753633.2:n.1805G>A
|
|
|
XR_001753634.2:n.1741G>A
|
|
|
NM_000400.4:c.1758G>A
MANE Select
|
NP_000391.1:p.Glu586=
|
|