ENST00000222747.8:c.409A>C
MANE Select
|
ENSP00000222747.3:p.Asn137His
|
|
ENST00000222747.7:c.409A>C
|
ENSP00000222747.3:p.Asn137His
|
|
ENST00000415871.5:c.409A>C
|
ENSP00000397699.1:p.Asn137His
|
|
ENST00000441017.5:c.409A>C
|
ENSP00000411158.1:p.Asn137His
|
|
ENST00000450414.5:c.388A>C
|
ENSP00000397411.1:n.388A>C
|
|
NM_012338.3:c.409A>C
|
NP_036470.1:p.Asn137His
|
|
XM_005250239.1:c.409A>C
|
XP_005250296.1:p.Asn137His
|
|
XM_011515993.1:c.409A>C
|
XP_011514295.1:p.Asn137His
|
|
XM_011515994.1:c.409A>C
|
XP_011514296.1:p.Asn137His
|
|
XM_005250239.3:c.409A>C
|
XP_005250296.1:p.Asn137His
|
|
XM_017011913.1:c.334A>C
|
XP_016867402.1:p.Asn112His
|
|
NM_012338.4:c.409A>C
MANE Select
|
NP_036470.1:p.Asn137His
|
|