ENST00000261304.7:c.664A=
MANE Select
|
ENSP00000261304.2:p.Lys222=
|
|
ENST00000261304.6:c.664A=
|
ENSP00000261304.2:p.Lys222=
|
|
ENST00000393568.8:c.595A=
|
ENSP00000377198.4:p.Lys199=
|
|
ENST00000393569.6:c.586A=
|
ENSP00000377199.2:p.Lys196=
|
|
ENST00000474294.6:n.654A=
|
|
|
ENST00000477716.3:n.419A=
|
|
|
ENST00000544807.6:c.496A=
|
ENSP00000437513.2:p.Lys166=
|
|
ENST00000554916.5:n.543A=
|
|
|
ENST00000555000.5:c.31A=
|
ENSP00000450472.1:p.Lys11=
|
|
ENST00000557316.5:c.*62A=
|
ENSP00000452314.1:n.*62A=
|
|
ENST00000622264.4:c.654A=
|
|
|
NM_000153.3:c.664A=
|
NP_000144.2:p.Lys222=
|
|
NM_001201401.1:c.595A=
|
NP_001188330.1:p.Lys199=
|
|
NM_001201402.1:c.586A=
|
NP_001188331.1:p.Lys196=
|
|
XM_011536618.1:c.496A=
|
XP_011534920.1:p.Lys166=
|
|
XM_011536618.2:c.496A=
|
XP_011534920.1:p.Lys166=
|
|
NM_000153.4:c.664A=
MANE Select
|
NP_000144.2:p.Lys222=
|
|
NM_001201401.2:c.595A=
|
NP_001188330.1:p.Lys199=
|
|
NM_001201402.2:c.586A=
|
NP_001188331.1:p.Lys196=
|
|