ENST00000527168.6:n.693G=
|
|
|
ENST00000529110.2:c.678G=
|
ENSP00000435349.2:p.Glu226=
|
|
ENST00000529957.6:n.652G=
|
|
|
ENST00000683366.1:c.*326G=
|
ENSP00000507283.1:n.*326G=
|
|
ENST00000683887.1:c.642G=
|
ENSP00000506886.1:p.Glu214=
|
|
ENST00000684100.1:n.588G=
|
|
|
ENST00000684126.1:n.652G=
|
|
|
ENST00000684688.1:n.1219G=
|
|
|
ENST00000204679.9:c.594G=
MANE Select
|
ENSP00000204679.4:p.Glu198=
|
|
ENST00000204679.8:c.594G=
|
ENSP00000204679.4:p.Glu198=
|
|
ENST00000527076.1:n.1741G=
|
|
|
ENST00000527168.5:n.761G=
|
|
|
ENST00000529957.5:n.693G=
|
|
|
NM_032520.4:c.594G=
|
NP_115909.1:p.Glu198=
|
|
XM_017023782.1:c.642G=
|
XP_016879271.1:p.Glu214=
|
|
XM_017023783.1:c.234G=
|
XP_016879272.1:p.Glu78=
|
|
NM_032520.5:c.594G=
MANE Select
|
NP_115909.1:p.Glu198=
|
|