ENST00000357750.9:c.840C>G
MANE Select
|
ENSP00000350387.4:p.Arg280=
|
|
ENST00000357750.8:c.840C>G
|
ENSP00000350387.4:p.Arg280=
|
|
ENST00000395139.7:c.840C>G
|
ENSP00000378571.3:p.Arg280=
|
|
ENST00000442581.1:c.840C>G
|
ENSP00000406657.1:p.Arg280=
|
|
ENST00000447092.5:c.840C>G
|
ENSP00000401853.1:p.Arg280=
|
|
ENST00000481597.5:n.975C>G
|
|
|
NM_003773.4:c.840C>G
|
NP_003764.3:p.Arg280=
|
|
NM_033158.4:c.840C>G
|
NP_149348.2:p.Arg280=
|
|
XM_005265524.1:c.840C>G
|
XP_005265581.1:p.Arg280=
|
|
XM_005265525.1:c.840C>G
|
XP_005265582.1:p.Arg280=
|
|
XM_005265524.2:c.840C>G
|
XP_005265581.1:p.Arg280=
|
|
XM_005265525.2:c.840C>G
|
XP_005265582.1:p.Arg280=
|
|
NM_003773.5:c.840C>G
MANE Select
|
NP_003764.3:p.Arg280=
|
|
NM_033158.5:c.840C>G
|
NP_149348.2:p.Arg280=
|
|