ENST00000527168.6:n.791A>G
|
|
|
ENST00000529110.2:c.776A>G
|
ENSP00000435349.2:p.Glu259Gly
|
|
ENST00000529957.6:n.750A>G
|
|
|
ENST00000683366.1:c.*424A>G
|
ENSP00000507283.1:n.*424A>G
|
|
ENST00000683887.1:c.740A>G
|
ENSP00000506886.1:p.Glu247Gly
|
|
ENST00000684100.1:n.686A>G
|
|
|
ENST00000684126.1:n.826A>G
|
|
|
ENST00000684688.1:n.1317A>G
|
|
|
ENST00000204679.9:c.692A>G
MANE Select
|
ENSP00000204679.4:p.Glu231Gly
|
|
ENST00000204679.8:c.692A>G
|
ENSP00000204679.4:p.Glu231Gly
|
|
ENST00000527076.1:n.1915A>G
|
|
|
ENST00000527168.5:n.859A>G
|
|
|
ENST00000529957.5:n.791A>G
|
|
|
NM_032520.4:c.692A>G
|
NP_115909.1:p.Glu231Gly
|
|
XM_017023782.1:c.740A>G
|
XP_016879271.1:p.Glu247Gly
|
|
XM_017023783.1:c.332A>G
|
XP_016879272.1:p.Glu111Gly
|
|
NM_032520.5:c.692A>G
MANE Select
|
NP_115909.1:p.Glu231Gly
|
|