ENST00000265104.5:c.11668G>A
MANE Select
|
ENSP00000265104.4:p.Glu3890Lys
|
|
ENST00000681290.1:c.11623G>A
|
ENSP00000505288.1:p.Glu3875Lys
|
|
ENST00000265104.4:c.11668G>A
|
ENSP00000265104.4:p.Glu3890Lys
|
|
NM_001369.2:c.11668G>A
|
NP_001360.1:p.Glu3890Lys
|
|
XM_005248262.2:c.11623G>A
|
XP_005248319.1:p.Glu3875Lys
|
|
XM_005248262.3:c.11776G>A
|
XP_005248319.2:p.Glu3926Lys
|
|
XM_017009177.1:c.11776G>A
|
XP_016864666.1:p.Glu3926Lys
|
|
XM_017009178.1:c.10681G>A
|
XP_016864667.1:p.Glu3561Lys
|
|
XM_017009179.2:c.10681G>A
|
XP_016864668.1:p.Glu3561Lys
|
|
XM_017009180.1:c.11776G>A
|
XP_016864669.1:p.Glu3926Lys
|
|
XM_017009181.1:c.11776G>A
|
XP_016864670.1:p.Glu3926Lys
|
|
XM_017009185.1:c.6865G>A
|
XP_016864674.1:p.Glu2289Lys
|
|
XM_017009186.1:c.6418G>A
|
XP_016864675.1:p.Glu2140Lys
|
|
XM_017009188.1:c.5755G>A
|
XP_016864677.1:p.Glu1919Lys
|
|
XM_024454388.1:c.10681G>A
|
XP_024310156.1:p.Glu3561Lys
|
|
XM_024454389.1:c.10270G>A
|
XP_024310157.1:p.Glu3424Lys
|
|
NM_001369.3:c.11668G>A
MANE Select
|
NP_001360.1:p.Glu3890Lys
|
|