ENST00000682565.1:c.10491C>T
|
ENSP00000507671.1:p.Ser3497=
|
|
ENST00000682801.1:c.10491C>T
|
ENSP00000507862.1:p.Ser3497=
|
|
ENST00000682859.1:c.10491C>T
|
ENSP00000508222.1:p.Ser3497=
|
|
ENST00000683791.1:c.3577C>T
|
|
|
ENST00000684460.1:c.7772C>T
|
|
|
ENST00000684548.1:c.10491C>T
|
ENSP00000507421.1:p.Ser3497=
|
|
ENST00000684590.1:c.4938C>T
|
ENSP00000507376.1:p.Ser1646=
|
|
ENST00000684656.1:c.7817C>T
|
|
|
ENST00000613296.6:c.10872C>T
MANE Select
|
ENSP00000482968.1:p.Ser3624=
|
|
ENST00000651057.1:c.1026C>T
|
ENSP00000498504.1:p.Ser342=
|
|
ENST00000651434.1:c.2228C>T
|
|
|
ENST00000651750.1:c.260C>T
|
|
|
ENST00000652487.1:c.1969C>T
|
|
|
ENST00000423048.5:c.4363C>T
|
ENSP00000399833.1:n.4363C>T
|
|
ENST00000484298.5:c.10746C>T
|
ENSP00000478155.1:p.Ser3582=
|
|
ENST00000613296.4:c.10872C>T
|
ENSP00000482968.1:p.Ser3624=
|
|
ENST00000614410.4:c.10872C>T
|
ENSP00000479094.1:p.Ser3624=
|
|
ENST00000620466.4:n.4675C>T
|
|
|
NM_015120.4:c.10875C>T , LRG_741t1:c.10875C>T
|
NP_055935.4:p.Ser3625=
|
|
NM_001378454.1:c.10872C>T
MANE Select
|
NP_001365383.1:p.Ser3624=
|
|