ENST00000231749.8:c.519G=
MANE Select
|
ENSP00000231749.3:p.Gln173=
|
|
ENST00000231749.7:c.519G=
|
ENSP00000231749.3:p.Gln173=
|
|
ENST00000360165.7:c.519G=
|
ENSP00000353289.3:p.Gln173=
|
|
ENST00000442887.1:c.390G=
|
ENSP00000393687.1:p.Gln130=
|
|
ENST00000443080.5:c.*271G=
|
ENSP00000415661.1:n.*271G=
|
|
ENST00000478269.5:n.604G=
|
|
|
NM_001308379.1:c.519G=
|
NP_001295308.1:p.Gln173=
|
|
NM_015896.2:c.519G=
|
NP_056980.2:p.Gln173=
|
|
NM_015896.3:c.519G=
|
NP_056980.2:p.Gln173=
|
|
XM_005265216.2:c.282G=
|
XP_005265273.1:p.Gln94=
|
|
XM_005265216.3:c.282G=
|
XP_005265273.1:p.Gln94=
|
|
NM_015896.4:c.519G=
MANE Select
|
NP_056980.2:p.Gln173=
|
|
NM_001308379.2:c.519G=
|
NP_001295308.1:p.Gln173=
|
|