ENST00000216361.9:c.1773G=
|
ENSP00000216361.5:p.Glu591=
|
|
ENST00000396618.9:c.1578G=
MANE Select
|
ENSP00000379862.3:p.Glu526=
|
|
ENST00000555117.2:c.1534+3404G=
|
ENSP00000493569.1:n.1534+3404G=
|
|
ENST00000643575.1:c.1578G=
|
ENSP00000494838.1:p.Glu526=
|
|
ENST00000643697.1:n.1880G=
|
|
|
ENST00000644874.2:c.1578G=
|
ENSP00000496360.1:p.Glu526=
|
|
ENST00000216361.8:c.1578G=
|
ENSP00000216361.4:p.Glu526=
|
|
ENST00000396618.7:c.1578G=
|
ENSP00000379862.3:p.Glu526=
|
|
ENST00000460581.6:c.1242G=
|
ENSP00000451713.1:p.Glu414=
|
|
ENST00000468826.2:c.1229G=
|
|
|
ENST00000475087.5:c.1477+3404G=
|
ENSP00000451528.1:n.1477+3404G=
|
|
NM_001135058.1:c.1578G=
|
NP_001128530.1:p.Glu526=
|
|
NM_004086.2:c.1578G=
|
NP_004077.1:p.Glu526=
|
|
NR_038356.1:n.93C=
|
|
|
XM_011536539.1:c.1578G=
|
XP_011534841.1:p.Glu526=
|
|
NM_001347720.1:c.1773G=
|
NP_001334649.1:p.Glu591=
|
|
XM_017021071.1:c.1773G=
|
XP_016876560.1:p.Glu591=
|
|
XM_024449506.1:c.1635G=
|
XP_024305274.1:p.Glu545=
|
|
NM_004086.3:c.1578G=
MANE Select
|
NP_004077.1:p.Glu526=
|
|
NM_001135058.2:c.1578G=
|
NP_001128530.1:p.Glu526=
|
|
NM_001347720.2:c.1773G=
|
NP_001334649.1:p.Glu591=
|
|