ENST00000527168.6:n.716A>G
|
|
|
ENST00000529110.2:c.701A>G
|
ENSP00000435349.2:p.Glu234Gly
|
|
ENST00000529957.6:n.675A>G
|
|
|
ENST00000683366.1:c.*349A>G
|
ENSP00000507283.1:n.*349A>G
|
|
ENST00000683887.1:c.665A>G
|
ENSP00000506886.1:p.Glu222Gly
|
|
ENST00000684100.1:n.611A>G
|
|
|
ENST00000684126.1:n.751A>G
|
|
|
ENST00000684688.1:n.1242A>G
|
|
|
ENST00000204679.9:c.617A>G
MANE Select
|
ENSP00000204679.4:p.Glu206Gly
|
|
ENST00000204679.8:c.617A>G
|
ENSP00000204679.4:p.Glu206Gly
|
|
ENST00000527076.1:n.1840A>G
|
|
|
ENST00000527168.5:n.784A>G
|
|
|
ENST00000529957.5:n.716A>G
|
|
|
NM_032520.4:c.617A>G
|
NP_115909.1:p.Glu206Gly
|
|
XM_017023782.1:c.665A>G
|
XP_016879271.1:p.Glu222Gly
|
|
XM_017023783.1:c.257A>G
|
XP_016879272.1:p.Glu86Gly
|
|
NM_032520.5:c.617A>G
MANE Select
|
NP_115909.1:p.Glu206Gly
|
|