|
NM_000829.4:c.1237G>C
MANE Select
|
NP_000820.4:p.Glu413Gln
|
|
ENST00000282499.10:c.1237G>C
MANE Select
|
ENSP00000282499.5:p.Glu413Gln
|
|
NM_000829.3:c.1237G>C
|
NP_000820.3:p.Glu413Gln
|
|
NM_001077243.2:c.1237G>C
|
NP_001070711.2:p.Glu413Gln
|
|
NM_001077243.3:c.1237G>C
|
NP_001070711.3:p.Glu413Gln
|
|
NM_001077244.1:c.1237G>C
|
NP_001070712.1:p.Glu413Gln
|
|
NM_001077244.2:c.1237G>C
|
NP_001070712.1:p.Glu413Gln
|
|
NM_001112812.1:c.1237G>C
|
NP_001106283.1:p.Glu413Gln
|
|
NM_001112812.2:c.1237G>C
|
NP_001106283.1:p.Glu413Gln
|
|
NR_046356.1:n.1551G>C
|
|
|
NR_046356.2:n.1529G>C
|
|
|
ENST00000282499.9:c.1237G>C
|
ENSP00000282499.5:p.Glu413Gln
|
|
ENST00000393125.6:c.1237G>C
|
ENSP00000376833.2:p.Glu413Gln
|
|
ENST00000393127.6:c.1237G>C
|
ENSP00000376835.2:p.Glu413Gln
|
|
ENST00000428631.6:c.1237G>C
|
ENSP00000415551.2:p.Glu413Gln
|
|
ENST00000525187.5:c.1237G>C
|
ENSP00000432180.1:p.Glu413Gln
|
|
ENST00000525187.6:c.1237G>C
|
ENSP00000432180.1:p.Glu413Gln
|
|
ENST00000530497.1:c.1237G>C
|
ENSP00000435775.1:p.Glu413Gln
|
|
ENST00000703743.2:c.1237G>C
|
ENSP00000515457.2:p.Glu413Gln
|
|
ENST00000706777.1:c.1237G>C
|
ENSP00000516542.1:p.Glu413Gln
|
|
XM_005271518.2:c.1237G>C
|
XP_005271575.1:p.Glu413Gln
|
|
XM_005271518.3:c.1237G>C
|
XP_005271575.1:p.Glu413Gln
|
|
XM_006718823.1:c.1237G>C
|
XP_006718886.1:p.Glu413Gln
|
|
XM_006718823.2:c.1237G>C
|
XP_006718886.1:p.Glu413Gln
|
|
XM_011542775.1:c.1237G>C
|
XP_011541077.1:p.Glu413Gln
|
|
XM_011542775.2:c.1237G>C
|
XP_011541077.1:p.Glu413Gln
|
|
XM_011542776.1:c.727G>C
|
XP_011541078.1:p.Glu243Gln
|
|
XM_011542776.3:c.727G>C
|
XP_011541078.1:p.Glu243Gln
|
|
XM_011542777.1:c.727G>C
|
XP_011541079.1:p.Glu243Gln
|
|
XM_011542777.3:c.727G>C
|
XP_011541079.1:p.Glu243Gln
|
|
XM_017017609.1:c.1237G>C
|
XP_016873098.1:p.Glu413Gln
|
|
XM_017017610.2:c.1237G>C
|
XP_016873099.1:p.Glu413Gln
|
|
XM_017017611.2:c.727G>C
|
XP_016873100.1:p.Glu243Gln
|
|
XM_024448454.1:c.1237G>C
|
XP_024304222.1:p.Glu413Gln
|
|
XM_024448455.1:c.1237G>C
|
XP_024304223.1:p.Glu413Gln
|
|
XR_001747841.1:n.1727G>C
|
|
|
XR_947825.1:n.1727G>C
|
|