ENST00000682565.1:c.10312A=
|
ENSP00000507671.1:p.Ser3438=
|
|
ENST00000682801.1:c.10312A=
|
ENSP00000507862.1:p.Ser3438=
|
|
ENST00000682859.1:c.10312A=
|
ENSP00000508222.1:p.Ser3438=
|
|
ENST00000683791.1:c.3398A=
|
|
|
ENST00000684460.1:c.7593A=
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|
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ENST00000684548.1:c.10312A=
|
ENSP00000507421.1:p.Ser3438=
|
|
ENST00000684590.1:c.4759A=
|
ENSP00000507376.1:p.Ser1587=
|
|
ENST00000684656.1:c.7638A=
|
|
|
ENST00000613296.6:c.10693A=
MANE Select
|
ENSP00000482968.1:p.Ser3565=
|
|
ENST00000651057.1:c.847A=
|
ENSP00000498504.1:p.Ser283=
|
|
ENST00000651434.1:c.2049A=
|
|
|
ENST00000651750.1:c.81A=
|
|
|
ENST00000652487.1:c.1790A=
|
|
|
ENST00000423048.5:c.4184A=
|
ENSP00000399833.1:n.4184A=
|
|
ENST00000484298.5:c.10567A=
|
ENSP00000478155.1:p.Ser3523=
|
|
ENST00000613296.4:c.10693A=
|
ENSP00000482968.1:p.Ser3565=
|
|
ENST00000614410.4:c.10693A=
|
ENSP00000479094.1:p.Ser3565=
|
|
ENST00000620466.4:n.4496A=
|
|
|
NM_015120.4:c.10696A= , LRG_741t1:c.10696A=
|
NP_055935.4:p.Ser3566=
|
|
NM_001378454.1:c.10693A=
MANE Select
|
NP_001365383.1:p.Ser3565=
|
|