ENST00000527168.6:n.828A>G
|
|
|
ENST00000529110.2:c.813A>G
|
ENSP00000435349.2:p.Glu271=
|
|
ENST00000529957.6:n.787A>G
|
|
|
ENST00000683366.1:c.*461A>G
|
ENSP00000507283.1:n.*461A>G
|
|
ENST00000683887.1:c.777A>G
|
ENSP00000506886.1:p.Glu259=
|
|
ENST00000684100.1:n.723A>G
|
|
|
ENST00000684126.1:n.863A>G
|
|
|
ENST00000684688.1:n.1354A>G
|
|
|
ENST00000204679.9:c.729A>G
MANE Select
|
ENSP00000204679.4:p.Glu243=
|
|
ENST00000204679.8:c.729A>G
|
ENSP00000204679.4:p.Glu243=
|
|
ENST00000527076.1:n.1952A>G
|
|
|
ENST00000527168.5:n.896A>G
|
|
|
ENST00000529957.5:n.828A>G
|
|
|
NM_032520.4:c.729A>G
|
NP_115909.1:p.Glu243=
|
|
XM_017023782.1:c.777A>G
|
XP_016879271.1:p.Glu259=
|
|
XM_017023783.1:c.369A>G
|
XP_016879272.1:p.Glu123=
|
|
NM_032520.5:c.729A>G
MANE Select
|
NP_115909.1:p.Glu243=
|
|