ENST00000369037.9:c.638A>T
MANE Select
|
ENSP00000358033.4:p.Glu213Val
|
|
ENST00000369037.8:c.638A>T
|
ENSP00000358033.4:p.Glu213Val
|
|
NM_020381.3:c.638A>T
|
NP_065114.3:p.Glu213Val
|
|
XM_011535956.1:c.638A>T
|
XP_011534258.1:p.Glu213Val
|
|
XM_011535957.1:c.638A>T
|
XP_011534259.1:p.Glu213Val
|
|
XM_011535958.1:c.503A>T
|
XP_011534260.1:p.Glu168Val
|
|
XM_011535959.1:c.638A>T
|
XP_011534261.1:p.Glu213Val
|
|
XM_011535960.1:c.230A>T
|
XP_011534262.1:p.Glu77Val
|
|
XM_011535961.1:c.638A>T
|
XP_011534263.1:p.Glu213Val
|
|
XM_011535962.1:c.230A>T
|
XP_011534264.1:p.Glu77Val
|
|
XM_011535956.3:c.638A>T
|
XP_011534258.1:p.Glu213Val
|
|
XM_011535957.3:c.638A>T
|
XP_011534259.1:p.Glu213Val
|
|
XM_011535958.3:c.503A>T
|
XP_011534260.1:p.Glu168Val
|
|
XM_011535959.3:c.638A>T
|
XP_011534261.1:p.Glu213Val
|
|
XM_011535960.3:c.230A>T
|
XP_011534262.1:p.Glu77Val
|
|
XM_011535961.3:c.638A>T
|
XP_011534263.1:p.Glu213Val
|
|
XM_011535962.2:c.230A>T
|
XP_011534264.1:p.Glu77Val
|
|
XM_017011082.2:c.638A>T
|
XP_016866571.1:p.Glu213Val
|
|
NM_020381.4:c.638A>T
MANE Select
|
NP_065114.3:p.Glu213Val
|
|