ENST00000328381.10:c.783A>G
MANE Select
|
ENSP00000328340.5:p.Pro261=
|
|
ENST00000324689.8:c.620A>G
|
ENSP00000323693.4:p.Gln207Arg
|
|
ENST00000328381.9:c.783A>G
|
ENSP00000328340.5:p.Pro261=
|
|
ENST00000443677.6:c.476A>G
|
ENSP00000411965.2:p.Gln159Arg
|
|
ENST00000535306.6:c.848A>G
|
ENSP00000440470.2:p.Gln283Arg
|
|
NM_001184992.1:c.848A>G
|
NP_001171921.1:p.Gln283Arg
|
|
NM_032322.3:c.783A>G
|
NP_115698.3:p.Pro261=
|
|
NM_197939.1:c.620A>G
|
NP_922921.1:p.Gln207Arg
|
|
XM_005258043.3:c.240A>G
|
XP_005258100.1:p.Pro80=
|
|
XM_006722138.2:c.462A>G
|
XP_006722201.1:p.Pro154=
|
|
XM_017025223.1:c.240A>G
|
XP_016880712.1:p.Pro80=
|
|
XM_024451000.1:c.240A>G
|
XP_024306768.1:p.Pro80=
|
|
XM_024451001.1:c.240A>G
|
XP_024306769.1:p.Pro80=
|
|
XR_002958076.1:n.1116A>G
|
|
|
XR_002958077.1:n.1051A>G
|
|
|
XR_002958078.1:n.888A>G
|
|
|
NM_032322.4:c.783A>G
MANE Select
|
NP_115698.3:p.Pro261=
|
|
NM_001184992.2:c.848A>G
|
NP_001171921.1:p.Gln283Arg
|
|
NM_197939.2:c.620A>G
|
NP_922921.1:p.Gln207Arg
|
|