ENST00000527168.6:n.528A>C
|
|
|
ENST00000529110.2:c.513A>C
|
ENSP00000435349.2:p.Gly171=
|
|
ENST00000529957.6:n.487A>C
|
|
|
ENST00000683366.1:c.*161A>C
|
ENSP00000507283.1:n.*161A>C
|
|
ENST00000683887.1:c.477A>C
|
ENSP00000506886.1:p.Gly159=
|
|
ENST00000684100.1:n.423A>C
|
|
|
ENST00000684126.1:n.487A>C
|
|
|
ENST00000684688.1:n.1054A>C
|
|
|
ENST00000204679.9:c.429A>C
MANE Select
|
ENSP00000204679.4:p.Gly143=
|
|
ENST00000204679.8:c.429A>C
|
ENSP00000204679.4:p.Gly143=
|
|
ENST00000527076.1:n.1445A>C
|
|
|
ENST00000527168.5:n.465A>C
|
|
|
ENST00000529110.1:c.496A>C
|
|
|
ENST00000529957.5:n.528A>C
|
|
|
NM_032520.4:c.429A>C
|
NP_115909.1:p.Gly143=
|
|
XM_017023782.1:c.477A>C
|
XP_016879271.1:p.Gly159=
|
|
XM_017023783.1:c.69A>C
|
XP_016879272.1:p.Gly23=
|
|
NM_032520.5:c.429A>C
MANE Select
|
NP_115909.1:p.Gly143=
|
|