ENST00000585465.3:c.*2790G=
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ENSP00000490268.2:n.*2790G=
|
|
ENST00000585748.3:c.817G=
|
ENSP00000477641.2:p.Ala273=
|
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ENST00000585851.2:c.1015G=
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ENSP00000467912.2:p.Ala339=
|
|
ENST00000326873.12:c.1189G=
MANE Select
|
ENSP00000324856.6:p.Ala397=
|
|
ENST00000326873.11:c.1189G=
|
ENSP00000324856.6:p.Ala397=
|
|
ENST00000585465.2:n.2922G=
|
|
|
ENST00000586243.5:c.1189G=
|
ENSP00000467240.2:p.Ala397=
|
|
ENST00000589152.5:n.1887G=
|
|
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NM_000455.4:c.1189G= , LRG_319t1:c.1189G=
|
NP_000446.1:p.Ala397=
|
|
XM_005259617.1:c.1184G=
|
XP_005259674.1:p.Gly395=
|
|
XM_011528209.1:c.962G=
|
XP_011526511.1:p.Gly321=
|
|
XM_005259617.3:c.1184G=
|
XP_005259674.1:p.Gly395=
|
|
XM_011528209.2:c.962G=
|
XP_011526511.1:p.Gly321=
|
|
XR_001753738.2:n.1995G=
|
|
|
XR_001753740.2:n.1965G=
|
|
|
NM_000455.5:c.1189G=
MANE Select
|
NP_000446.1:p.Ala397=
|
|