ENST00000491895.7:c.567T=
MANE Select
|
ENSP00000419045.2:p.Ile189=
|
|
ENST00000254299.8:n.715T=
|
|
|
ENST00000395514.5:c.567T=
|
ENSP00000378890.1:p.Ile189=
|
|
ENST00000395521.6:n.293-2773T=
|
|
|
ENST00000491895.6:c.567T=
|
ENSP00000419045.2:p.Ile189=
|
|
ENST00000536224.2:c.567T=
|
ENSP00000445246.2:p.Ile189=
|
|
ENST00000543643.6:c.567T=
|
ENSP00000444011.2:p.Ile189=
|
|
ENST00000622544.4:c.567T=
|
ENSP00000477796.1:p.Ile189=
|
|
NM_000161.2:c.567T=
|
NP_000152.1:p.Ile189=
|
|
NM_001024024.1:c.567T=
|
NP_001019195.1:p.Ile189=
|
|
NM_001024070.1:c.567T=
|
NP_001019241.1:p.Ile189=
|
|
NM_001024071.1:c.567T=
|
NP_001019242.1:p.Ile189=
|
|
XM_005267530.1:c.567T=
|
XP_005267587.1:p.Ile189=
|
|
XM_017021218.1:c.273T=
|
XP_016876707.1:p.Ile91=
|
|
NM_000161.3:c.567T=
MANE Select
|
NP_000152.1:p.Ile189=
|
|
NM_001024070.2:c.567T=
|
NP_001019241.1:p.Ile189=
|
|
NM_001024071.2:c.567T=
|
NP_001019242.1:p.Ile189=
|
|
NM_001024024.2:c.567T=
|
NP_001019195.1:p.Ile189=
|
|