ENST00000525748.6:c.1434A>G
MANE Select
|
ENSP00000434364.2:p.Leu478=
|
|
ENST00000298923.11:c.*731A>G
|
ENSP00000298923.7:n.*731A>G
|
|
ENST00000525748.5:c.1434A>G
|
ENSP00000434364.1:p.Leu478=
|
|
NM_004211.3:c.1434A>G
|
NP_004202.2:p.Leu478=
|
|
XM_005253225.1:c.732A>G
|
XP_005253282.1:p.Leu244=
|
|
XM_011520473.1:c.1434A>G
|
XP_011518775.1:p.Leu478=
|
|
NM_001318369.1:c.732A>G
|
NP_001305298.1:p.Leu244=
|
|
NM_004211.4:c.1434A>G
|
NP_004202.3:p.Leu478=
|
|
XM_017018544.2:c.558A>G
|
XP_016874033.1:p.Leu186=
|
|
XM_017018545.2:c.393A>G
|
XP_016874034.1:p.Leu131=
|
|
NM_001318369.2:c.732A>G
|
NP_001305298.1:p.Leu244=
|
|
NM_004211.5:c.1434A>G
MANE Select
|
NP_004202.4:p.Leu478=
|
|