ENST00000400521.7:c.822G>A
MANE Select
|
ENSP00000383365.1:p.Arg274=
|
|
ENST00000334363.14:c.822G>A
|
ENSP00000334451.9:p.Arg274=
|
|
ENST00000400518.5:c.732G>A
|
ENSP00000383362.1:p.Arg244=
|
|
ENST00000400519.6:c.819G>A
|
ENSP00000383363.1:p.Arg273=
|
|
ENST00000400521.6:c.822G>A
|
ENSP00000383365.1:p.Arg274=
|
|
ENST00000400525.6:c.753G>A
|
ENSP00000383369.3:p.Arg251=
|
|
ENST00000474308.5:c.765G>A
|
ENSP00000485665.1:p.Arg255=
|
|
ENST00000475995.3:c.319G>A
|
|
|
ENST00000491939.6:c.726G>A
|
ENSP00000485543.1:p.Arg242=
|
|
ENST00000494454.5:n.896G>A
|
|
|
ENST00000542719.6:c.534G>A
|
ENSP00000485128.2:p.Arg178=
|
|
ENST00000634537.1:c.51G>A
|
ENSP00000489208.1:p.Arg17=
|
|
ENST00000635155.1:n.408G>A
|
|
|
NM_001282512.1:c.822G>A
|
NP_001269441.1:p.Arg274=
|
|
NM_006440.4:c.822G>A
|
NP_006431.2:p.Arg274=
|
|
NM_001282512.2:c.822G>A
|
NP_001269441.1:p.Arg274=
|
|
NM_001352300.1:c.819G>A
|
NP_001339229.1:p.Arg273=
|
|
NM_001352301.1:c.732G>A
|
NP_001339230.1:p.Arg244=
|
|
NM_001352302.1:c.534G>A
|
NP_001339231.1:p.Arg178=
|
|
NM_001352303.1:c.726G>A
|
NP_001339232.1:p.Arg242=
|
|
NR_147957.1:n.954G>A
|
|
|
NM_006440.5:c.822G>A
MANE Select
|
NP_006431.2:p.Arg274=
|
|
NM_001282512.3:c.822G>A
|
NP_001269441.1:p.Arg274=
|
|
NM_001352300.2:c.819G>A
|
NP_001339229.1:p.Arg273=
|
|
NR_147957.2:n.780G>A
|
|
|
NM_001352301.2:c.732G>A
|
NP_001339230.1:p.Arg244=
|
|
NM_001352302.2:c.534G>A
|
NP_001339231.1:p.Arg178=
|
|
NM_001352303.2:c.726G>A
|
NP_001339232.1:p.Arg242=
|
|