ENST00000461073.6:c.*2728A>G
|
ENSP00000419905.1:n.*2728A>G
|
|
ENST00000485349.6:n.4156A>G
|
|
|
ENST00000491994.2:c.*222A>G
|
ENSP00000417586.2:n.*222A>G
|
|
ENST00000494058.6:n.3982A>G
|
|
|
ENST00000697831.1:c.3611A>G
|
ENSP00000513453.1:p.Glu1204Gly
|
|
ENST00000697832.1:n.3833A>G
|
|
|
ENST00000697834.1:n.4398A>G
|
|
|
ENST00000697835.1:c.*3198A>G
|
ENSP00000513455.1:n.*3198A>G
|
|
ENST00000697836.1:n.4034A>G
|
|
|
ENST00000697837.1:c.*796A>G
|
ENSP00000513456.1:n.*796A>G
|
|
ENST00000697838.1:c.3545A>G
|
ENSP00000513457.1:p.Glu1182Gly
|
|
ENST00000697839.1:n.4492A>G
|
|
|
ENST00000697840.1:c.3716A>G
|
ENSP00000513458.1:p.Glu1239Gly
|
|
ENST00000697841.1:n.4591A>G
|
|
|
ENST00000697842.1:n.3935A>G
|
|
|
ENST00000375394.7:c.3680A>G
MANE Select
|
ENSP00000364543.2:p.Glu1227Gly
|
|
ENST00000375394.6:c.3680A>G
|
ENSP00000364543.2:p.Glu1227Gly
|
|
ENST00000465703.5:n.4410A>G
|
|
|
ENST00000471818.1:n.609A>G
|
|
|
ENST00000474839.5:c.*3052A>G
|
ENSP00000420470.1:n.*3052A>G
|
|
ENST00000483553.5:c.1210A>G
|
|
|
ENST00000491994.1:c.769A>G
|
|
|
NM_006929.4:c.3680A>G
|
NP_008860.4:p.Glu1227Gly
|
|
XR_926301.3:n.3696A>G
|
|
|
NM_006929.5:c.3680A>G
MANE Select
|
NP_008860.4:p.Glu1227Gly
|
|