ENST00000592793.6:n.3191A>G
|
|
|
ENST00000682020.1:c.461A>G
|
ENSP00000508075.1:p.Asp154Gly
|
|
ENST00000682206.1:c.*147A>G
|
ENSP00000508285.1:n.*147A>G
|
|
ENST00000682314.1:n.1103A>G
|
|
|
ENST00000682327.1:c.527A>G
|
ENSP00000507058.1:p.Asp176Gly
|
|
ENST00000682349.1:n.3197A>G
|
|
|
ENST00000682703.1:n.4023A>G
|
|
|
ENST00000682797.1:c.*147A>G
|
ENSP00000507582.1:n.*147A>G
|
|
ENST00000682985.1:c.566A>G
|
ENSP00000507598.1:p.Asp189Gly
|
|
ENST00000683433.1:c.311A>G
|
ENSP00000507463.1:p.Asp104Gly
|
|
ENST00000683685.1:n.1929A>G
|
|
|
ENST00000683710.1:c.*1022A>G
|
ENSP00000506785.1:n.*1022A>G
|
|
ENST00000683739.1:c.722A>G
|
ENSP00000507002.1:p.Asp241Gly
|
|
ENST00000683772.1:n.1099A>G
|
|
|
ENST00000684008.1:c.993A>G
|
ENSP00000507962.1:n.993A>G
|
|
ENST00000684190.1:c.1016A>G
|
ENSP00000507554.1:p.Asp339Gly
|
|
ENST00000684335.1:c.961+1232A>G
|
ENSP00000508112.1:n.961+1232A>G
|
|
ENST00000262374.10:c.1055A>G
MANE Select
|
ENSP00000262374.5:p.Asp352Gly
|
|
ENST00000650085.1:n.1879A>G
|
|
|
ENST00000262374.9:c.1055A>G
|
ENSP00000262374.4:p.Asp352Gly
|
|
ENST00000544428.1:c.722A>G
|
ENSP00000440019.1:p.Asp241Gly
|
|
ENST00000588623.5:c.722A>G
|
ENSP00000468118.1:p.Asp241Gly
|
|
ENST00000591822.5:c.*956A>G
|
ENSP00000467865.1:n.*956A>G
|
|
NM_019109.4:c.1055A>G
|
NP_061982.3:p.Asp352Gly
|
|
XM_011522565.1:c.722A>G
|
XP_011520867.1:p.Asp241Gly
|
|
NM_001330504.1:c.722A>G
|
NP_001317433.1:p.Asp241Gly
|
|
XM_017023457.2:c.1016A>G
|
XP_016878946.1:p.Asp339Gly
|
|
XM_017023458.1:c.722A>G
|
XP_016878947.1:p.Asp241Gly
|
|
XR_932882.3:n.1084A>G
|
|
|
NM_019109.5:c.1055A>G
MANE Select
|
NP_061982.3:p.Asp352Gly
|
|
NM_001330504.2:c.722A>G
|
NP_001317433.1:p.Asp241Gly
|
|