ENST00000222747.8:c.807G>A
MANE Select
|
ENSP00000222747.3:p.Gln269=
|
|
ENST00000222747.7:c.807G>A
|
ENSP00000222747.3:p.Gln269=
|
|
ENST00000415871.5:c.807G>A
|
ENSP00000397699.1:p.Gln269=
|
|
ENST00000450414.5:c.786G>A
|
ENSP00000397411.1:n.786G>A
|
|
NM_012338.3:c.807G>A
|
NP_036470.1:p.Gln269=
|
|
XM_005250239.1:c.807G>A
|
XP_005250296.1:p.Gln269=
|
|
XM_011515993.1:c.807G>A
|
XP_011514295.1:p.Gln269=
|
|
XM_011515994.1:c.807G>A
|
XP_011514296.1:p.Gln269=
|
|
XM_005250239.3:c.807G>A
|
XP_005250296.1:p.Gln269=
|
|
XM_017011913.1:c.732G>A
|
XP_016867402.1:p.Gln244=
|
|
NM_012338.4:c.807G>A
MANE Select
|
NP_036470.1:p.Gln269=
|
|