ENST00000585465.3:c.691T=
|
ENSP00000490268.2:p.Phe231=
|
|
ENST00000585748.3:c.319T=
|
ENSP00000477641.2:p.Phe107=
|
|
ENST00000585851.2:c.517T=
|
ENSP00000467912.2:p.Phe173=
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|
ENST00000326873.12:c.691T=
MANE Select
|
ENSP00000324856.6:p.Phe231=
|
|
ENST00000652231.1:c.691T=
|
ENSP00000498804.1:p.Phe231=
|
|
ENST00000326873.11:c.691T=
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ENSP00000324856.6:p.Phe231=
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|
ENST00000586243.5:c.691T=
|
ENSP00000467240.2:p.Phe231=
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|
ENST00000586358.5:n.589T=
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|
|
ENST00000589152.5:n.781T=
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|
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ENST00000591133.2:n.662T=
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|
|
NM_000455.4:c.691T= , LRG_319t1:c.691T=
|
NP_000446.1:p.Phe231=
|
|
XM_005259617.1:c.691T=
|
XP_005259674.1:p.Phe231=
|
|
XM_005259618.3:c.691T=
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XP_005259675.1:p.Phe231=
|
|
XM_011528209.1:c.469T=
|
XP_011526511.1:p.Phe157=
|
|
XR_936204.1:n.1316T=
|
|
|
XM_005259617.3:c.691T=
|
XP_005259674.1:p.Phe231=
|
|
XM_011528209.2:c.469T=
|
XP_011526511.1:p.Phe157=
|
|
XR_001753738.2:n.1316T=
|
|
|
XR_001753739.1:n.1316T=
|
|
|
XR_001753740.2:n.1316T=
|
|
|
NM_000455.5:c.691T=
MANE Select
|
NP_000446.1:p.Phe231=
|
|