ENST00000292408.9:c.1658C>G
MANE Select
|
ENSP00000292408.4:p.Ala553Gly
|
|
ENST00000292408.8:c.1658C>G
|
ENSP00000292408.4:p.Ala553Gly
|
|
ENST00000393637.5:c.1538C>G
|
ENSP00000377254.1:p.Ala513Gly
|
|
ENST00000393648.6:c.1454C>G
|
ENSP00000377259.2:p.Ala485Gly
|
|
ENST00000483872.2:n.644C>G
|
|
|
ENST00000502906.5:c.1658C>G
|
ENSP00000424960.1:p.Ala553Gly
|
|
ENST00000511076.1:c.552C>G
|
|
|
NM_001291980.1:c.1454C>G
|
NP_001278909.1:p.Ala485Gly
|
|
NM_002011.4:c.1658C>G
|
NP_002002.3:p.Ala553Gly
|
|
NM_022963.3:c.1538C>G
|
NP_075252.2:p.Ala513Gly
|
|
NM_213647.2:c.1658C>G
|
NP_998812.1:p.Ala553Gly
|
|
XM_005265838.2:c.1658C>G
|
XP_005265895.1:p.Ala553Gly
|
|
XM_011534464.1:c.1751C>G
|
XP_011532766.1:p.Ala584Gly
|
|
XM_011534465.1:c.1340C>G
|
XP_011532767.1:p.Ala447Gly
|
|
XR_941090.1:n.1653C>G
|
|
|
NM_001354984.1:c.1658C>G
|
NP_001341913.1:p.Ala553Gly
|
|
NM_213647.3:c.1658C>G
MANE Select
|
NP_998812.1:p.Ala553Gly
|
|
NM_001291980.2:c.1454C>G
|
NP_001278909.1:p.Ala485Gly
|
|
NM_001354984.2:c.1658C>G
|
NP_001341913.1:p.Ala553Gly
|
|
NM_002011.5:c.1658C>G
|
NP_002002.3:p.Ala553Gly
|
|