ENST00000372811.10:c.537G>A
MANE Select
|
ENSP00000361898.6:p.Arg179=
|
|
ENST00000372809.5:c.576G>A
|
ENSP00000361895.5:p.Arg192=
|
|
ENST00000372811.9:c.537G>A
|
ENSP00000361898.5:p.Arg179=
|
|
ENST00000420632.6:c.69G>A
|
ENSP00000391261.2:p.Arg23=
|
|
ENST00000434861.5:c.531G>A
|
ENSP00000407606.1:p.Arg177=
|
|
ENST00000469745.5:n.449G>A
|
|
|
ENST00000480630.5:n.1184G>A
|
|
|
ENST00000483824.5:n.672G>A
|
|
|
NM_001136493.2:c.576G>A
|
NP_001129965.1:p.Arg192=
|
|
NM_001287808.1:c.69G>A
|
NP_001274737.1:p.Arg23=
|
|
NM_001287809.1:c.426G>A
|
NP_001274738.1:p.Arg142=
|
|
NM_032793.4:c.537G>A
|
NP_116182.2:p.Arg179=
|
|
NR_109896.1:n.718G>A
|
|
|
XM_005271285.1:c.531G>A
|
XP_005271342.1:p.Arg177=
|
|
XM_011542312.1:c.537G>A
|
XP_011540614.1:p.Arg179=
|
|
XR_946783.1:n.685G>A
|
|
|
NM_001349821.1:c.531G>A
|
NP_001336750.1:p.Arg177=
|
|
NM_001349822.1:c.537G>A
|
NP_001336751.1:p.Arg179=
|
|
NM_001349823.1:c.192G>A
|
NP_001336752.1:p.Arg64=
|
|
NM_001136493.3:c.576G>A
|
NP_001129965.1:p.Arg192=
|
|
NM_001287809.2:c.426G>A
|
NP_001274738.1:p.Arg142=
|
|
NM_001349821.2:c.531G>A
|
NP_001336750.1:p.Arg177=
|
|
NM_001349822.2:c.537G>A
|
NP_001336751.1:p.Arg179=
|
|
NM_001349823.2:c.192G>A
|
NP_001336752.1:p.Arg64=
|
|
NM_032793.5:c.537G>A
MANE Select
|
NP_116182.2:p.Arg179=
|
|
NR_109896.2:n.685G>A
|
|
|
NM_001287808.2:c.69G>A
|
NP_001274737.1:p.Arg23=
|
|