ENST00000682565.1:c.10611T>C
|
ENSP00000507671.1:p.Ser3537=
|
|
ENST00000682801.1:c.10611T>C
|
ENSP00000507862.1:p.Ser3537=
|
|
ENST00000682859.1:c.10611T>C
|
ENSP00000508222.1:p.Ser3537=
|
|
ENST00000683791.1:c.3697T>C
|
|
|
ENST00000684460.1:c.7892T>C
|
|
|
ENST00000684548.1:c.10611T>C
|
ENSP00000507421.1:p.Ser3537=
|
|
ENST00000684590.1:c.5058T>C
|
ENSP00000507376.1:p.Ser1686=
|
|
ENST00000684656.1:c.7937T>C
|
|
|
ENST00000613296.6:c.10992T>C
MANE Select
|
ENSP00000482968.1:p.Ser3664=
|
|
ENST00000651057.1:c.1146T>C
|
ENSP00000498504.1:p.Ser382=
|
|
ENST00000651434.1:c.2348T>C
|
|
|
ENST00000651750.1:c.380T>C
|
|
|
ENST00000652487.1:c.2089T>C
|
|
|
ENST00000423048.5:c.4483T>C
|
ENSP00000399833.1:n.4483T>C
|
|
ENST00000484298.5:c.10866T>C
|
ENSP00000478155.1:p.Ser3622=
|
|
ENST00000613296.4:c.10992T>C
|
ENSP00000482968.1:p.Ser3664=
|
|
ENST00000614410.4:c.10992T>C
|
ENSP00000479094.1:p.Ser3664=
|
|
ENST00000620466.4:n.4795T>C
|
|
|
NM_015120.4:c.10995T>C , LRG_741t1:c.10995T>C
|
NP_055935.4:p.Ser3665=
|
|
NM_001378454.1:c.10992T>C
MANE Select
|
NP_001365383.1:p.Ser3664=
|
|