ENST00000265104.5:c.10724A>G
MANE Select
|
ENSP00000265104.4:p.Glu3575Gly
|
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ENST00000681290.1:c.10679A>G
|
ENSP00000505288.1:p.Glu3560Gly
|
|
ENST00000265104.4:c.10724A>G
|
ENSP00000265104.4:p.Glu3575Gly
|
|
NM_001369.2:c.10724A>G
|
NP_001360.1:p.Glu3575Gly
|
|
XM_005248262.2:c.10679A>G
|
XP_005248319.1:p.Glu3560Gly
|
|
XM_005248262.3:c.10832A>G
|
XP_005248319.2:p.Glu3611Gly
|
|
XM_017009177.1:c.10832A>G
|
XP_016864666.1:p.Glu3611Gly
|
|
XM_017009178.1:c.9737A>G
|
XP_016864667.1:p.Glu3246Gly
|
|
XM_017009179.2:c.9737A>G
|
XP_016864668.1:p.Glu3246Gly
|
|
XM_017009180.1:c.10832A>G
|
XP_016864669.1:p.Glu3611Gly
|
|
XM_017009181.1:c.10832A>G
|
XP_016864670.1:p.Glu3611Gly
|
|
XM_017009182.1:c.10832A>G
|
XP_016864671.1:p.Glu3611Gly
|
|
XM_017009185.1:c.5921A>G
|
XP_016864674.1:p.Glu1974Gly
|
|
XM_017009186.1:c.5474A>G
|
XP_016864675.1:p.Glu1825Gly
|
|
XM_017009188.1:c.4811A>G
|
XP_016864677.1:p.Glu1604Gly
|
|
XM_024454388.1:c.9737A>G
|
XP_024310156.1:p.Glu3246Gly
|
|
XM_024454389.1:c.9326A>G
|
XP_024310157.1:p.Glu3109Gly
|
|
NM_001369.3:c.10724A>G
MANE Select
|
NP_001360.1:p.Glu3575Gly
|
|