ENST00000231749.8:c.89A>T
MANE Select
|
ENSP00000231749.3:p.Glu30Val
|
|
ENST00000231749.7:c.89A>T
|
ENSP00000231749.3:p.Glu30Val
|
|
ENST00000360165.7:c.89A>T
|
ENSP00000353289.3:p.Glu30Val
|
|
ENST00000431869.1:c.89A>T
|
ENSP00000391545.1:p.Glu30Val
|
|
ENST00000442887.1:c.-38+44A>T
|
ENSP00000393687.1:n.-38+44A>T
|
|
ENST00000443080.5:c.89A>T
|
ENSP00000415661.1:p.Glu30Val
|
|
ENST00000468182.1:n.191A>T
|
|
|
NM_001308379.1:c.89A>T
|
NP_001295308.1:p.Glu30Val
|
|
NM_015896.2:c.89A>T
|
NP_056980.2:p.Glu30Val
|
|
NM_015896.3:c.89A>T
|
NP_056980.2:p.Glu30Val
|
|
XM_005265216.2:c.-40A>T
|
XP_005265273.1:n.-40A>T
|
|
XM_005265216.3:c.-40A>T
|
XP_005265273.1:n.-40A>T
|
|
NM_015896.4:c.89A>T
MANE Select
|
NP_056980.2:p.Glu30Val
|
|
NM_001308379.2:c.89A>T
|
NP_001295308.1:p.Glu30Val
|
|