ENST00000682565.1:c.11558C=
|
ENSP00000507671.1:p.Thr3853=
|
|
ENST00000682801.1:c.11167-924C=
|
ENSP00000507862.1:n.11167-924C=
|
|
ENST00000682859.1:c.11558C=
|
ENSP00000508222.1:p.Thr3853=
|
|
ENST00000683791.1:c.4644C=
|
|
|
ENST00000684460.1:c.8839C=
|
|
|
ENST00000684548.1:c.11558C=
|
ENSP00000507421.1:p.Thr3853=
|
|
ENST00000684590.1:c.6005C=
|
ENSP00000507376.1:p.Thr2002=
|
|
ENST00000684656.1:c.9023C=
|
|
|
ENST00000613296.6:c.11939C=
MANE Select
|
ENSP00000482968.1:p.Thr3980=
|
|
ENST00000651057.1:c.2093C=
|
ENSP00000498504.1:p.Thr698=
|
|
ENST00000651434.1:c.3295C=
|
|
|
ENST00000651750.1:c.1260+380C=
|
|
|
ENST00000652487.1:c.3110C=
|
|
|
ENST00000464408.3:n.114C=
|
|
|
ENST00000484298.5:c.11813C=
|
ENSP00000478155.1:p.Thr3938=
|
|
ENST00000613296.4:c.11939C=
|
ENSP00000482968.1:p.Thr3980=
|
|
ENST00000620466.4:n.5742C=
|
|
|
NM_015120.4:c.11942C= , LRG_741t1:c.11942C=
|
NP_055935.4:p.Thr3981=
|
|
NM_001378454.1:c.11939C=
MANE Select
|
NP_001365383.1:p.Thr3980=
|
|