ENST00000265104.5:c.9844G>A
MANE Select
|
ENSP00000265104.4:p.Glu3282Lys
|
|
ENST00000681290.1:c.9799G>A
|
ENSP00000505288.1:p.Glu3267Lys
|
|
ENST00000265104.4:c.9844G>A
|
ENSP00000265104.4:p.Glu3282Lys
|
|
ENST00000504001.3:n.556G>A
|
|
|
NM_001369.2:c.9844G>A
|
NP_001360.1:p.Glu3282Lys
|
|
XM_005248262.2:c.9799G>A
|
XP_005248319.1:p.Glu3267Lys
|
|
XM_005248262.3:c.9952G>A
|
XP_005248319.2:p.Glu3318Lys
|
|
XM_017009177.1:c.9952G>A
|
XP_016864666.1:p.Glu3318Lys
|
|
XM_017009178.1:c.8857G>A
|
XP_016864667.1:p.Glu2953Lys
|
|
XM_017009179.2:c.8857G>A
|
XP_016864668.1:p.Glu2953Lys
|
|
XM_017009180.1:c.9952G>A
|
XP_016864669.1:p.Glu3318Lys
|
|
XM_017009181.1:c.9952G>A
|
XP_016864670.1:p.Glu3318Lys
|
|
XM_017009182.1:c.9952G>A
|
XP_016864671.1:p.Glu3318Lys
|
|
XM_017009185.1:c.5041G>A
|
XP_016864674.1:p.Glu1681Lys
|
|
XM_017009186.1:c.4594G>A
|
XP_016864675.1:p.Glu1532Lys
|
|
XM_017009188.1:c.3931G>A
|
XP_016864677.1:p.Glu1311Lys
|
|
XM_024454388.1:c.8857G>A
|
XP_024310156.1:p.Glu2953Lys
|
|
XM_024454389.1:c.8446G>A
|
XP_024310157.1:p.Glu2816Lys
|
|
NM_001369.3:c.9844G>A
MANE Select
|
NP_001360.1:p.Glu3282Lys
|
|