ENST00000339818.9:c.339C>A
MANE Select
|
ENSP00000344566.4:p.Arg113=
|
|
ENST00000325223.7:c.339C>A
|
ENSP00000317302.7:p.Arg113=
|
|
ENST00000339818.8:c.339C>A
|
ENSP00000344566.4:p.Arg113=
|
|
ENST00000397956.7:c.339C>A
|
ENSP00000381047.3:p.Arg113=
|
|
ENST00000462742.1:n.2510C>A
|
|
|
ENST00000478674.1:n.398C>A
|
|
|
ENST00000496321.5:n.455C>A
|
|
|
NM_001271440.1:c.339C>A
|
NP_001258369.1:p.Arg113=
|
|
NM_001271441.1:c.339C>A
|
NP_001258370.1:p.Arg113=
|
|
NM_001271442.1:c.216C>A
|
NP_001258371.1:p.Arg72=
|
|
NM_004928.2:c.339C>A
|
NP_004919.1:p.Arg113=
|
|
XM_006724051.2:c.414C>A
|
XP_006724114.1:p.Arg138=
|
|
XM_006724052.2:c.414C>A
|
XP_006724115.1:p.Arg138=
|
|
XM_006724053.2:c.15C>A
|
XP_006724116.1:p.Arg5=
|
|
XR_937571.1:n.542C>A
|
|
|
XM_006724051.3:c.414C>A
|
XP_006724114.1:p.Arg138=
|
|
XM_006724053.3:c.15C>A
|
XP_006724116.1:p.Arg5=
|
|
XM_017028470.1:c.543C>A
|
XP_016883959.1:p.Arg181=
|
|
XM_017028471.1:c.288C>A
|
XP_016883960.1:p.Arg96=
|
|
XM_017028472.1:c.15C>A
|
XP_016883961.1:p.Arg5=
|
|
XR_937571.2:n.549C>A
|
|
|
NM_004928.3:c.339C>A
MANE Select
|
NP_004919.1:p.Arg113=
|
|
NM_001271440.2:c.339C>A
|
NP_001258369.1:p.Arg113=
|
|
NM_001271441.2:c.339C>A
|
NP_001258370.1:p.Arg113=
|
|