ENST00000298229.7:c.937G>C
MANE Select
|
ENSP00000298229.2:p.Glu313Gln
|
|
ENST00000298229.6:c.937G>C
|
ENSP00000298229.2:p.Glu313Gln
|
|
ENST00000538751.5:c.211G>C
|
ENSP00000444619.1:p.Glu71Gln
|
|
ENST00000540329.5:c.121G>C
|
ENSP00000440018.1:p.Glu41Gln
|
|
ENST00000541756.5:c.739G>C
|
ENSP00000446360.2:p.Glu247Gln
|
|
NM_001567.3:c.937G>C
|
NP_001558.3:p.Glu313Gln
|
|
XM_005273978.3:c.1003G>C
|
XP_005274035.1:p.Glu335Gln
|
|
XM_005273979.3:c.1003G>C
|
XP_005274036.1:p.Glu335Gln
|
|
XM_011544999.1:c.937G>C
|
XP_011543301.1:p.Glu313Gln
|
|
XM_011545000.1:c.1003G>C
|
XP_011543302.1:p.Glu335Gln
|
|
XM_005273979.4:c.1003G>C
|
XP_005274036.1:p.Glu335Gln
|
|
XM_011544999.2:c.937G>C
|
XP_011543301.1:p.Glu313Gln
|
|
XM_024448501.1:c.1003G>C
|
XP_024304269.1:p.Glu335Gln
|
|
XM_024448502.1:c.1003G>C
|
XP_024304270.1:p.Glu335Gln
|
|
XM_024448503.1:c.973G>C
|
XP_024304271.1:p.Glu325Gln
|
|
XM_024448504.1:c.937G>C
|
XP_024304272.1:p.Glu313Gln
|
|
XM_024448505.1:c.1003G>C
|
XP_024304273.1:p.Glu335Gln
|
|
NM_001567.4:c.937G>C
MANE Select
|
NP_001558.3:p.Glu313Gln
|
|