ENST00000689298.1:c.*457C>G
|
ENSP00000508434.1:n.*457C>G
|
|
ENST00000440875.6:c.-170C>G
|
ENSP00000475553.3:n.-170C>G
|
|
ENST00000627532.3:c.608C>G
MANE Select
|
ENSP00000487174.1:p.Thr203Ser
|
|
ENST00000636026.2:c.608C>G
|
ENSP00000490776.1:p.Thr203Ser
|
|
ENST00000636179.1:n.577C>G
|
|
|
ENST00000636413.1:c.272C>G
|
ENSP00000490508.1:p.Thr91Ser
|
|
ENST00000636471.1:c.608C>G
|
ENSP00000490317.1:p.Thr203Ser
|
|
ENST00000636732.2:c.*325C>G
|
ENSP00000490175.1:n.*325C>G
|
|
ENST00000636820.1:n.708C>G
|
|
|
ENST00000637045.1:c.272C>G
|
ENSP00000490141.1:p.Thr91Ser
|
|
ENST00000637267.2:c.608C>G
|
ENSP00000490293.2:p.Thr203Ser
|
|
ENST00000637304.1:c.272C>G
|
ENSP00000490872.1:p.Thr91Ser
|
|
ENST00000638007.1:c.272C>G
|
ENSP00000490723.1:p.Thr91Ser
|
|
ENST00000638087.1:c.272C>G
|
ENSP00000490673.1:p.Thr91Ser
|
|
ENST00000638128.1:c.-170C>G
|
ENSP00000490934.1:n.-170C>G
|
|
ENST00000675069.1:c.-133-5265C>G
|
ENSP00000502467.1:n.-133-5265C>G
|
|
ENST00000303660.8:c.605C>G
|
ENSP00000302501.4:p.Thr202Ser
|
|
ENST00000392861.6:c.692C>G
|
ENSP00000376601.3:p.Thr231Ser
|
|
ENST00000409487.7:c.608C>G
|
ENSP00000386854.2:p.Thr203Ser
|
|
ENST00000419938.5:c.347C>G
|
ENSP00000394777.2:p.Thr116Ser
|
|
ENST00000427902.5:c.695C>G
|
ENSP00000395496.2:p.Thr232Ser
|
|
ENST00000431672.4:c.536C>G
|
ENSP00000475267.2:p.Thr179Ser
|
|
ENST00000440875.5:c.593C>G
|
ENSP00000475553.2:p.Thr198Ser
|
|
ENST00000497268.1:n.554C>G
|
|
|
ENST00000539609.7:c.536C>G
|
ENSP00000443792.2:p.Thr179Ser
|
|
ENST00000558170.6:c.608C>G
|
ENSP00000454157.1:p.Thr203Ser
|
|
ENST00000627532.2:c.608C>G
|
ENSP00000487174.1:p.Thr203Ser
|
|
ENST00000627856.2:n.568C>G
|
|
|
NM_001171653.1:c.536C>G
|
NP_001165124.1:p.Thr179Ser
|
|
NM_014795.3:c.608C>G
|
NP_055610.1:p.Thr203Ser
|
|
XM_006712881.2:c.608C>G
|
XP_006712944.1:p.Thr203Ser
|
|
XM_006712882.2:c.608C>G
|
XP_006712945.1:p.Thr203Ser
|
|
XM_011512231.1:c.599C>G
|
XP_011510533.1:p.Thr200Ser
|
|
XM_011512232.1:c.587C>G
|
XP_011510534.1:p.Thr196Ser
|
|
NM_014795.4:c.608C>G
MANE Select
|
NP_055610.1:p.Thr203Ser
|
|
NM_001171653.2:c.536C>G
|
NP_001165124.1:p.Thr179Ser
|
|