ENST00000682565.1:c.10055C>G
|
ENSP00000507671.1:p.Ser3352Ter
|
|
ENST00000682801.1:c.10055C>G
|
ENSP00000507862.1:p.Ser3352Ter
|
|
ENST00000682859.1:c.10055C>G
|
ENSP00000508222.1:p.Ser3352Ter
|
|
ENST00000683791.1:c.3141C>G
|
|
|
ENST00000684460.1:c.7336C>G
|
|
|
ENST00000684548.1:c.10055C>G
|
ENSP00000507421.1:p.Ser3352Ter
|
|
ENST00000684590.1:c.4502C>G
|
ENSP00000507376.1:p.Ser1501Ter
|
|
ENST00000684656.1:c.7381C>G
|
|
|
ENST00000613296.6:c.10436C>G
MANE Select
|
ENSP00000482968.1:p.Ser3479Ter
|
|
ENST00000651057.1:c.590C>G
|
ENSP00000498504.1:p.Ser197Ter
|
|
ENST00000651434.1:c.1792C>G
|
|
|
ENST00000652487.1:c.1533C>G
|
|
|
ENST00000423048.5:c.3927C>G
|
ENSP00000399833.1:n.3927C>G
|
|
ENST00000484298.5:c.10310C>G
|
ENSP00000478155.1:p.Ser3437Ter
|
|
ENST00000613296.4:c.10436C>G
|
ENSP00000482968.1:p.Ser3479Ter
|
|
ENST00000614410.4:c.10436C>G
|
ENSP00000479094.1:p.Ser3479Ter
|
|
ENST00000620466.4:n.4239C>G
|
|
|
NM_015120.4:c.10439C>G , LRG_741t1:c.10439C>G
|
NP_055935.4:p.Ser3480Ter
|
|
NM_001378454.1:c.10436C>G
MANE Select
|
NP_001365383.1:p.Ser3479Ter
|
|