ENST00000400521.7:c.836G>A
MANE Select
|
ENSP00000383365.1:p.Cys279Tyr
|
|
ENST00000334363.14:c.836G>A
|
ENSP00000334451.9:p.Cys279Tyr
|
|
ENST00000400518.5:c.746G>A
|
ENSP00000383362.1:p.Cys249Tyr
|
|
ENST00000400519.6:c.833G>A
|
ENSP00000383363.1:p.Cys278Tyr
|
|
ENST00000400521.6:c.836G>A
|
ENSP00000383365.1:p.Cys279Tyr
|
|
ENST00000400525.6:c.767G>A
|
ENSP00000383369.3:p.Cys256Tyr
|
|
ENST00000474308.5:c.779G>A
|
ENSP00000485665.1:p.Cys260Tyr
|
|
ENST00000475995.3:c.333G>A
|
|
|
ENST00000491939.6:c.740G>A
|
ENSP00000485543.1:p.Cys247Tyr
|
|
ENST00000494454.5:n.910G>A
|
|
|
ENST00000542719.6:c.548G>A
|
ENSP00000485128.2:p.Cys183Tyr
|
|
ENST00000634537.1:c.65G>A
|
ENSP00000489208.1:p.Cys22Tyr
|
|
ENST00000635155.1:n.422G>A
|
|
|
NM_001282512.1:c.836G>A
|
NP_001269441.1:p.Cys279Tyr
|
|
NM_006440.4:c.836G>A
|
NP_006431.2:p.Cys279Tyr
|
|
NM_001282512.2:c.836G>A
|
NP_001269441.1:p.Cys279Tyr
|
|
NM_001352300.1:c.833G>A
|
NP_001339229.1:p.Cys278Tyr
|
|
NM_001352301.1:c.746G>A
|
NP_001339230.1:p.Cys249Tyr
|
|
NM_001352302.1:c.548G>A
|
NP_001339231.1:p.Cys183Tyr
|
|
NM_001352303.1:c.740G>A
|
NP_001339232.1:p.Cys247Tyr
|
|
NR_147957.1:n.968G>A
|
|
|
NM_006440.5:c.836G>A
MANE Select
|
NP_006431.2:p.Cys279Tyr
|
|
NM_001282512.3:c.836G>A
|
NP_001269441.1:p.Cys279Tyr
|
|
NM_001352300.2:c.833G>A
|
NP_001339229.1:p.Cys278Tyr
|
|
NR_147957.2:n.794G>A
|
|
|
NM_001352301.2:c.746G>A
|
NP_001339230.1:p.Cys249Tyr
|
|
NM_001352302.2:c.548G>A
|
NP_001339231.1:p.Cys183Tyr
|
|
NM_001352303.2:c.740G>A
|
NP_001339232.1:p.Cys247Tyr
|
|