ENST00000265404.7:c.497A>C
MANE Select
|
ENSP00000265404.2:p.Glu166Ala
|
|
ENST00000265404.6:c.497A>C
|
ENSP00000265404.2:p.Glu166Ala
|
|
ENST00000396225.1:c.497A>C
|
ENSP00000379527.1:p.Glu166Ala
|
|
NM_012108.2:c.497A>C
|
NP_036240.1:p.Glu166Ala
|
|
XM_005265675.3:c.497A>C
|
XP_005265732.1:p.Glu166Ala
|
|
XM_006714175.2:c.497A>C
|
XP_006714238.1:p.Glu166Ala
|
|
XR_427541.2:n.555A>C
|
|
|
NM_001317769.1:c.497A>C
|
NP_001304698.1:p.Glu166Ala
|
|
NM_012108.3:c.497A>C
|
NP_036240.1:p.Glu166Ala
|
|
XM_017008018.2:c.497A>C
|
XP_016863507.1:p.Glu166Ala
|
|
NM_012108.4:c.497A>C
MANE Select
|
NP_036240.1:p.Glu166Ala
|
|
NM_001317769.2:c.497A>C
|
NP_001304698.1:p.Glu166Ala
|
|