ENST00000682565.1:c.11725A=
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ENSP00000507671.1:p.Thr3909=
|
|
ENST00000682801.1:c.11167-757A=
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ENSP00000507862.1:n.11167-757A=
|
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ENST00000682859.1:c.11725A=
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ENSP00000508222.1:p.Thr3909=
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|
ENST00000683791.1:c.4811A=
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|
|
ENST00000684460.1:c.9006A=
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|
|
ENST00000684548.1:c.11725A=
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ENSP00000507421.1:p.Thr3909=
|
|
ENST00000684590.1:c.6172A=
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ENSP00000507376.1:p.Thr2058=
|
|
ENST00000684656.1:c.9190A=
|
|
|
ENST00000613296.6:c.12106A=
MANE Select
|
ENSP00000482968.1:p.Thr4036=
|
|
ENST00000651057.1:c.2260A=
|
ENSP00000498504.1:p.Thr754=
|
|
ENST00000651434.1:c.3462A=
|
|
|
ENST00000651750.1:c.1260+547A=
|
|
|
ENST00000652487.1:c.3277A=
|
|
|
ENST00000464408.3:n.281A=
|
|
|
ENST00000484298.5:c.11980A=
|
ENSP00000478155.1:p.Thr3994=
|
|
ENST00000613296.4:c.12106A=
|
ENSP00000482968.1:p.Thr4036=
|
|
ENST00000620466.4:n.5909A=
|
|
|
NM_015120.4:c.12109A= , LRG_741t1:c.12109A=
|
NP_055935.4:p.Thr4037=
|
|
NM_001378454.1:c.12106A=
MANE Select
|
NP_001365383.1:p.Thr4036=
|
|