ENST00000392666.6:c.266A>T
MANE Select
|
ENSP00000376434.1:p.Asp89Val
|
|
ENST00000324003.3:c.266A>T
|
ENSP00000316136.3:p.Asp89Val
|
|
ENST00000324036.7:c.266A>T
|
ENSP00000316233.3:p.Asp89Val
|
|
ENST00000392664.2:c.323A>T
|
ENSP00000376432.2:p.Asp108Val
|
|
ENST00000392665.6:c.266A>T
|
ENSP00000376433.2:p.Asp89Val
|
|
ENST00000392666.5:c.266A>T
|
ENSP00000376434.1:p.Asp89Val
|
|
ENST00000440599.6:c.266A>T
|
ENSP00000406320.2:p.Asp89Val
|
|
NM_000220.4:c.323A>T
|
NP_000211.1:p.Asp108Val
|
|
NM_153764.2:c.266A>T
|
NP_722448.1:p.Asp89Val
|
|
NM_153765.2:c.317A>T
|
NP_722449.3:p.Asp106Val
|
|
NM_153766.2:c.266A>T
|
NP_722450.1:p.Asp89Val
|
|
NM_153767.3:c.266A>T
|
NP_722451.1:p.Asp89Val
|
|
NM_000220.6:c.323A>T
|
NP_000211.1:p.Asp108Val
|
|
NM_153764.3:c.266A>T
|
NP_722448.1:p.Asp89Val
|
|
NM_153765.3:c.317A>T
|
NP_722449.3:p.Asp106Val
|
|
NM_153766.3:c.266A>T
MANE Select
|
NP_722450.1:p.Asp89Val
|
|
NM_153767.4:c.266A>T
|
NP_722451.1:p.Asp89Val
|
|