ENST00000222747.8:c.413A=
MANE Select
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ENSP00000222747.3:p.Tyr138=
|
|
ENST00000222747.7:c.413A=
|
ENSP00000222747.3:p.Tyr138=
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|
ENST00000415871.5:c.413A=
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ENSP00000397699.1:p.Tyr138=
|
|
ENST00000441017.5:c.413A=
|
ENSP00000411158.1:p.Tyr138=
|
|
ENST00000450414.5:c.392A=
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ENSP00000397411.1:n.392A=
|
|
NM_012338.3:c.413A=
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NP_036470.1:p.Tyr138=
|
|
XM_005250239.1:c.413A=
|
XP_005250296.1:p.Tyr138=
|
|
XM_011515993.1:c.413A=
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XP_011514295.1:p.Tyr138=
|
|
XM_011515994.1:c.413A=
|
XP_011514296.1:p.Tyr138=
|
|
XM_005250239.3:c.413A=
|
XP_005250296.1:p.Tyr138=
|
|
XM_017011913.1:c.338A=
|
XP_016867402.1:p.Tyr113=
|
|
NM_012338.4:c.413A=
MANE Select
|
NP_036470.1:p.Tyr138=
|
|