ENST00000357578.8:c.1227T>G
MANE Select
|
ENSP00000350191.3:p.Gly409=
|
|
ENST00000479394.2:n.342T>G
|
|
|
ENST00000672352.1:c.846T>G
|
ENSP00000500876.1:p.Gly282=
|
|
ENST00000672652.1:c.1190T>G
|
|
|
ENST00000348925.2:c.1266T>G
|
ENSP00000314649.3:p.Gly422=
|
|
ENST00000357578.7:c.1227T>G
|
ENSP00000350191.3:p.Gly409=
|
|
ENST00000479394.1:n.342T>G
|
|
|
ENST00000491546.5:c.1143T>G
|
ENSP00000417687.1:p.Gly381=
|
|
NM_001080.3:c.1227T>G
MANE Select
|
NP_001071.1:p.Gly409=
|
|
NM_170740.1:c.1266T>G
|
NP_733936.1:p.Gly422=
|
|
NM_001368954.1:c.1083T>G
|
NP_001355883.1:p.Gly361=
|
|