ENST00000682565.1:c.10260C>T
|
ENSP00000507671.1:p.Ser3420=
|
|
ENST00000682801.1:c.10260C>T
|
ENSP00000507862.1:p.Ser3420=
|
|
ENST00000682859.1:c.10260C>T
|
ENSP00000508222.1:p.Ser3420=
|
|
ENST00000683791.1:c.3346C>T
|
|
|
ENST00000684460.1:c.7541C>T
|
|
|
ENST00000684548.1:c.10260C>T
|
ENSP00000507421.1:p.Ser3420=
|
|
ENST00000684590.1:c.4707C>T
|
ENSP00000507376.1:p.Ser1569=
|
|
ENST00000684656.1:c.7586C>T
|
|
|
ENST00000613296.6:c.10641C>T
MANE Select
|
ENSP00000482968.1:p.Ser3547=
|
|
ENST00000651057.1:c.795C>T
|
ENSP00000498504.1:p.Ser265=
|
|
ENST00000651434.1:c.1997C>T
|
|
|
ENST00000651750.1:c.29C>T
|
|
|
ENST00000652487.1:c.1738C>T
|
|
|
ENST00000423048.5:c.4132C>T
|
ENSP00000399833.1:n.4132C>T
|
|
ENST00000484298.5:c.10515C>T
|
ENSP00000478155.1:p.Ser3505=
|
|
ENST00000613296.4:c.10641C>T
|
ENSP00000482968.1:p.Ser3547=
|
|
ENST00000614410.4:c.10641C>T
|
ENSP00000479094.1:p.Ser3547=
|
|
ENST00000620466.4:n.4444C>T
|
|
|
NM_015120.4:c.10644C>T , LRG_741t1:c.10644C>T
|
NP_055935.4:p.Ser3548=
|
|
NM_001378454.1:c.10641C>T
MANE Select
|
NP_001365383.1:p.Ser3547=
|
|