ENST00000302475.9:c.1608G=
|
ENSP00000305617.4:p.Gln536=
|
|
ENST00000408903.7:c.2178G=
MANE Select
|
ENSP00000386227.3:p.Gln726=
|
|
ENST00000302475.8:c.1608G=
|
ENSP00000305617.4:p.Gln536=
|
|
ENST00000408903.6:c.2178G=
|
ENSP00000386227.3:p.Gln726=
|
|
ENST00000514701.5:c.1608G=
|
ENSP00000485220.1:p.Gln536=
|
|
ENST00000515367.6:c.1419G=
|
ENSP00000421615.2:p.Gln473=
|
|
ENST00000624689.3:c.22G=
|
|
|
NM_001085377.1:c.2178G=
|
NP_001078846.1:p.Gln726=
|
|
NM_002387.2:c.1608G=
|
NP_002378.1:p.Gln536=
|
|
XM_005271991.2:c.1608G=
|
XP_005272048.1:p.Gln536=
|
|
XM_005271991.3:c.1608G=
|
XP_005272048.1:p.Gln536=
|
|
XM_017009473.1:c.2178G=
|
XP_016864962.1:p.Gln726=
|
|
XM_017009474.1:c.1578G=
|
XP_016864963.1:p.Gln526=
|
|
XM_024446049.1:c.1419G=
|
XP_024301817.1:p.Gln473=
|
|
XM_024446050.1:c.1419G=
|
XP_024301818.1:p.Gln473=
|
|
XM_024446051.1:c.1419G=
|
XP_024301819.1:p.Gln473=
|
|
XM_024446052.1:c.1419G=
|
XP_024301820.1:p.Gln473=
|
|
NM_001085377.2:c.2178G=
MANE Select
|
NP_001078846.2:p.Gln726=
|
|
NM_002387.3:c.1608G=
|
NP_002378.2:p.Gln536=
|
|