ENST00000400521.7:c.921C>G
MANE Select
|
ENSP00000383365.1:p.Gly307=
|
|
ENST00000334363.14:c.921C>G
|
ENSP00000334451.9:p.Gly307=
|
|
ENST00000400518.5:c.831C>G
|
ENSP00000383362.1:p.Gly277=
|
|
ENST00000400519.6:c.918C>G
|
ENSP00000383363.1:p.Gly306=
|
|
ENST00000400521.6:c.921C>G
|
ENSP00000383365.1:p.Gly307=
|
|
ENST00000400525.6:c.852C>G
|
ENSP00000383369.3:p.Gly284=
|
|
ENST00000474308.5:c.864C>G
|
ENSP00000485665.1:p.Gly288=
|
|
ENST00000475995.3:c.418C>G
|
|
|
ENST00000491939.6:c.825C>G
|
ENSP00000485543.1:p.Gly275=
|
|
ENST00000494454.5:n.995C>G
|
|
|
ENST00000542719.6:c.633C>G
|
ENSP00000485128.2:p.Gly211=
|
|
ENST00000634537.1:c.150C>G
|
ENSP00000489208.1:p.Gly50=
|
|
ENST00000635155.1:n.507C>G
|
|
|
NM_001282512.1:c.921C>G
|
NP_001269441.1:p.Gly307=
|
|
NM_006440.4:c.921C>G
|
NP_006431.2:p.Gly307=
|
|
NM_001282512.2:c.921C>G
|
NP_001269441.1:p.Gly307=
|
|
NM_001352300.1:c.918C>G
|
NP_001339229.1:p.Gly306=
|
|
NM_001352301.1:c.831C>G
|
NP_001339230.1:p.Gly277=
|
|
NM_001352302.1:c.633C>G
|
NP_001339231.1:p.Gly211=
|
|
NM_001352303.1:c.825C>G
|
NP_001339232.1:p.Gly275=
|
|
NR_147957.1:n.1053C>G
|
|
|
NM_006440.5:c.921C>G
MANE Select
|
NP_006431.2:p.Gly307=
|
|
NM_001282512.3:c.921C>G
|
NP_001269441.1:p.Gly307=
|
|
NM_001352300.2:c.918C>G
|
NP_001339229.1:p.Gly306=
|
|
NR_147957.2:n.879C>G
|
|
|
NM_001352301.2:c.831C>G
|
NP_001339230.1:p.Gly277=
|
|
NM_001352302.2:c.633C>G
|
NP_001339231.1:p.Gly211=
|
|
NM_001352303.2:c.825C>G
|
NP_001339232.1:p.Gly275=
|
|