ENST00000693473.1:c.2658A>G
|
|
|
ENST00000371113.9:c.2541A>G
MANE Select
|
ENSP00000360154.4:p.Leu847=
|
|
ENST00000646010.1:c.2589A>G
|
|
|
ENST00000646914.1:c.1846A>G
|
|
|
ENST00000647245.1:c.2092A>G
|
|
|
ENST00000357121.5:c.2517A>G
|
ENSP00000349635.5:p.Leu839=
|
|
ENST00000371113.8:c.2541A>G
|
ENSP00000360154.4:p.Leu847=
|
|
ENST00000463271.1:n.328A>G
|
|
|
NM_000276.3:c.2541A>G
|
NP_000267.2:p.Leu847=
|
|
NM_001587.3:c.2517A>G
|
NP_001578.2:p.Leu839=
|
|
XM_005262422.1:c.2070A>G
|
XP_005262479.1:p.Leu690=
|
|
XM_011531342.1:c.2544A>G
|
XP_011529644.1:p.Leu848=
|
|
XM_011531343.1:c.2520A>G
|
XP_011529645.1:p.Leu840=
|
|
XM_011531344.1:c.2397A>G
|
XP_011529646.1:p.Leu799=
|
|
XM_011531345.1:c.2397A>G
|
XP_011529647.1:p.Leu799=
|
|
NM_001318784.1:c.2544A>G
|
NP_001305713.1:p.Leu848=
|
|
XM_005262422.2:c.2070A>G
|
XP_005262479.1:p.Leu690=
|
|
XM_011531344.3:c.2397A>G
|
XP_011529646.1:p.Leu799=
|
|
XM_011531345.3:c.2397A>G
|
XP_011529647.1:p.Leu799=
|
|
NM_000276.4:c.2541A>G
MANE Select
|
NP_000267.2:p.Leu847=
|
|
NM_001318784.2:c.2544A>G
|
NP_001305713.1:p.Leu848=
|
|
NM_001587.4:c.2517A>G
|
NP_001578.2:p.Leu839=
|
|