|
ENST00000689298.1:c.*527G>T
|
ENSP00000508434.1:n.*527G>T
|
|
|
ENST00000440875.6:c.-100G>T
|
ENSP00000475553.3:n.-100G>T
|
|
|
ENST00000627532.3:c.678G>T
MANE Select
|
ENSP00000487174.1:p.Leu226=
|
|
|
ENST00000636026.2:c.678G>T
|
ENSP00000490776.1:p.Leu226=
|
|
|
ENST00000636179.1:n.647G>T
|
|
|
|
ENST00000636413.1:c.342G>T
|
ENSP00000490508.1:p.Leu114=
|
|
|
ENST00000636471.1:c.678G>T
|
ENSP00000490317.1:p.Leu226=
|
|
|
ENST00000636732.2:c.*395G>T
|
ENSP00000490175.1:n.*395G>T
|
|
|
ENST00000636820.1:n.778G>T
|
|
|
|
ENST00000637045.1:c.342G>T
|
ENSP00000490141.1:p.Leu114=
|
|
|
ENST00000637267.2:c.678G>T
|
ENSP00000490293.2:p.Leu226=
|
|
|
ENST00000637304.1:c.342G>T
|
ENSP00000490872.1:p.Leu114=
|
|
|
ENST00000638007.1:c.342G>T
|
ENSP00000490723.1:p.Leu114=
|
|
|
ENST00000638087.1:c.342G>T
|
ENSP00000490673.1:p.Leu114=
|
|
|
ENST00000638128.1:c.-100G>T
|
ENSP00000490934.1:n.-100G>T
|
|
|
ENST00000675069.1:c.-133-5195G>T
|
ENSP00000502467.1:n.-133-5195G>T
|
|
|
ENST00000303660.8:c.675G>T
|
ENSP00000302501.4:p.Leu225=
|
|
|
ENST00000392861.6:c.762G>T
|
ENSP00000376601.3:p.Leu254=
|
|
|
ENST00000409487.7:c.678G>T
|
ENSP00000386854.2:p.Leu226=
|
|
|
ENST00000419938.5:c.417G>T
|
ENSP00000394777.2:p.Leu139=
|
|
|
ENST00000427902.5:c.765G>T
|
ENSP00000395496.2:p.Leu255=
|
|
|
ENST00000440875.5:c.663G>T
|
ENSP00000475553.2:p.Leu221=
|
|
|
ENST00000497268.1:n.624G>T
|
|
|
|
ENST00000539609.7:c.606G>T
|
ENSP00000443792.2:p.Leu202=
|
|
|
ENST00000558170.6:c.678G>T
|
ENSP00000454157.1:p.Leu226=
|
|
|
ENST00000627532.2:c.678G>T
|
ENSP00000487174.1:p.Leu226=
|
|
|
NM_001171653.1:c.606G>T
|
NP_001165124.1:p.Leu202=
|
|
|
NM_014795.3:c.678G>T
|
NP_055610.1:p.Leu226=
|
|
|
XM_006712881.2:c.678G>T
|
XP_006712944.1:p.Leu226=
|
|
|
XM_006712882.2:c.678G>T
|
XP_006712945.1:p.Leu226=
|
|
|
XM_011512231.1:c.669G>T
|
XP_011510533.1:p.Leu223=
|
|
|
XM_011512232.1:c.657G>T
|
XP_011510534.1:p.Leu219=
|
|
|
NM_014795.4:c.678G>T
MANE Select
|
NP_055610.1:p.Leu226=
|
|
|
NM_001171653.2:c.606G>T
|
NP_001165124.1:p.Leu202=
|
|
