ENST00000355832.10:c.3497A>T
MANE Select
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ENSP00000348089.5:p.Glu1166Val
|
|
ENST00000679552.1:n.568A>T
|
|
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ENST00000679871.1:n.643A>T
|
|
|
ENST00000679974.1:n.546A>T
|
|
|
ENST00000681632.1:n.4900A>T
|
|
|
ENST00000681659.1:c.3338A>T
|
ENSP00000505631.1:p.Glu1113Val
|
|
ENST00000355832.9:c.3497A>T
|
ENSP00000348089.5:p.Glu1166Val
|
|
ENST00000623073.3:c.*1793A>T
|
ENSP00000485650.1:n.*1793A>T
|
|
ENST00000623115.3:c.1607A>T
|
ENSP00000485321.1:p.Glu536Val
|
|
ENST00000624341.3:c.1329A>T
|
|
|
NM_000124.3:c.3497A>T
|
NP_000115.1:p.Glu1166Val
|
|
XR_945953.1:n.243-1102T>A
|
|
|
NM_001346440.1:c.3497A>T
|
NP_001333369.1:p.Glu1166Val
|
|
NM_000124.4:c.3497A>T
MANE Select
|
NP_000115.1:p.Glu1166Val
|
|
NM_001346440.2:c.3497A>T
|
NP_001333369.1:p.Glu1166Val
|
|