|
ENST00000370695.8:c.651T>A
|
ENSP00000359729.4:p.Leu217=
|
|
|
ENST00000370701.6:c.495T>A
|
ENSP00000359735.1:p.Leu165=
|
|
|
ENST00000630721.3:c.495T>A
MANE Select
|
ENSP00000487486.2:p.Leu165=
|
|
|
ENST00000636092.1:c.495T>A
|
ENSP00000490406.1:p.Leu165=
|
|
|
ENST00000636347.1:c.495T>A
|
ENSP00000490648.1:p.Leu165=
|
|
|
ENST00000637195.1:c.399T>A
|
ENSP00000490330.1:p.Leu133=
|
|
|
ENST00000637234.1:c.495T>A
|
ENSP00000490527.1:p.Leu165=
|
|
|
ENST00000637581.1:c.495T>A
|
ENSP00000490731.1:p.Leu165=
|
|
|
ENST00000643775.1:n.438T>A
|
|
|
|
ENST00000674809.1:c.438T>A
|
ENSP00000502455.1:p.Leu146=
|
|
|
ENST00000675550.1:n.436T>A
|
|
|
|
ENST00000675856.1:n.438T>A
|
|
|
|
ENST00000676043.1:c.438T>A
|
ENSP00000501920.1:p.Leu146=
|
|
|
ENST00000678163.1:c.651T>A
|
ENSP00000502845.1:p.Leu217=
|
|
|
ENST00000370695.6:c.651T>A
|
ENSP00000359729.4:p.Leu217=
|
|
|
ENST00000370698.7:c.555T>A
|
ENSP00000359732.3:p.Leu185=
|
|
|
ENST00000370701.5:c.495T>A
|
ENSP00000359735.1:p.Leu165=
|
|
|
ENST00000627534.2:c.495T>A
|
ENSP00000486743.1:p.Leu165=
|
|
|
NM_001042537.1:c.651T>A
|
NP_001036002.1:p.Leu217=
|
|
|
NM_001177651.1:c.495T>A
|
NP_001171122.1:p.Leu165=
|
|
|
NM_006359.2:c.555T>A
|
NP_006350.1:p.Leu185=
|
|
|
XM_006724726.2:c.495T>A
|
XP_006724789.1:p.Leu165=
|
|
|
XM_011531243.1:c.399T>A
|
XP_011529545.1:p.Leu133=
|
|
|
NM_001330652.1:c.399T>A
|
NP_001317581.1:p.Leu133=
|
|
|
XM_006724726.3:c.495T>A
|
XP_006724789.1:p.Leu165=
|
|
|
XM_017029223.2:c.495T>A
|
XP_016884712.1:p.Leu165=
|
|
|
XM_017029224.1:c.495T>A
|
XP_016884713.1:p.Leu165=
|
|
|
XM_017029225.1:c.399T>A
|
XP_016884714.1:p.Leu133=
|
|
|
NM_001177651.2:c.495T>A
|
NP_001171122.1:p.Leu165=
|
|
|
NM_001330652.2:c.399T>A
|
NP_001317581.1:p.Leu133=
|
|
|
NM_006359.3:c.555T>A
|
NP_006350.1:p.Leu185=
|
|
|
NM_001042537.2:c.651T>A
|
NP_001036002.1:p.Leu217=
|
|
|
NM_001379110.1:c.495T>A
MANE Select
|
NP_001366039.1:p.Leu165=
|
|
|
NM_001400909.1:c.495T>A
|
NP_001387838.1:p.Leu165=
|
|
|
NM_001400910.1:c.495T>A
|
NP_001387839.1:p.Leu165=
|
|
|
NM_001400911.1:c.495T>A
|
NP_001387840.1:p.Leu165=
|
|
|
NM_001400912.1:c.495T>A
|
NP_001387841.1:p.Leu165=
|
|
|
NM_001400913.1:c.399T>A
|
NP_001387842.1:p.Leu133=
|
|
