ENST00000635540.2:c.*208A>G
|
ENSP00000489185.1:n.*208A>G
|
|
ENST00000399799.3:c.3573A>G
MANE Select
|
ENSP00000382697.1:p.Glu1191=
|
|
ENST00000399799.2:c.3573A>G
|
ENSP00000382697.1:p.Glu1191=
|
|
ENST00000584687.1:n.283A>G
|
|
|
ENST00000635540.1:c.*208A>G
|
ENSP00000489185.1:n.*208A>G
|
|
NM_005406.2:c.3573A>G
|
NP_005397.1:p.Glu1191=
|
|
XM_011526136.1:c.3651A>G
|
XP_011524438.1:p.Glu1217=
|
|
XM_011526137.1:c.2184A>G
|
XP_011524439.1:p.Glu728=
|
|
XM_011526137.3:c.2184A>G
|
XP_011524439.1:p.Glu728=
|
|
NM_005406.3:c.3573A>G
MANE Select
|
NP_005397.1:p.Glu1191=
|
|