ENST00000338468.8:c.412+61389A=
|
ENSP00000343589.4:n.412+61389A=
|
|
ENST00000366894.6:c.288A=
|
ENSP00000355860.2:p.Ter96=
|
|
ENST00000366898.6:c.529A=
MANE Select
|
ENSP00000355865.1:p.Thr177=
|
|
ENST00000673871.1:c.524A=
|
|
|
ENST00000674232.1:n.547A=
|
|
|
ENST00000674436.1:n.165A=
|
|
|
ENST00000674501.1:n.636A=
|
|
|
ENST00000338468.7:c.-40+61389A=
|
ENSP00000343589.3:n.-40+61389A=
|
|
ENST00000366892.5:c.529A=
|
ENSP00000355858.1:p.Thr177=
|
|
ENST00000366894.5:c.-45A=
|
ENSP00000355860.1:n.-45A=
|
|
ENST00000366896.5:c.172-227719A=
|
ENSP00000355862.1:n.172-227719A=
|
|
ENST00000366897.5:c.529A=
|
ENSP00000355863.1:p.Thr177=
|
|
ENST00000366898.5:c.529A=
|
ENSP00000355865.1:p.Thr177=
|
|
ENST00000479615.5:c.292A=
|
ENSP00000434414.1:p.Thr98=
|
|
NM_004562.2:c.529A=
|
NP_004553.2:p.Thr177=
|
|
NM_013987.2:c.529A=
|
NP_054642.2:p.Thr177=
|
|
NM_013988.2:c.172-227719A=
|
NP_054643.2:n.172-227719A=
|
|
XM_011535863.1:c.526A=
|
XP_011534165.1:p.Thr176=
|
|
XM_011535864.1:c.529A=
|
XP_011534166.1:p.Thr177=
|
|
XM_011535865.1:c.529A=
|
XP_011534167.1:p.Thr177=
|
|
XM_011535866.1:c.529A=
|
XP_011534168.1:p.Thr177=
|
|
XM_011535867.1:c.529A=
|
XP_011534169.1:p.Thr177=
|
|
XM_017010908.1:c.643A=
|
XP_016866397.1:p.Thr215=
|
|
XM_017010909.2:c.289A=
|
XP_016866398.1:p.Thr97=
|
|
XM_024446449.1:c.292A=
|
XP_024302217.1:p.Thr98=
|
|
XR_001743443.2:n.635A=
|
|
|
NM_004562.3:c.529A=
MANE Select
|
NP_004553.2:p.Thr177=
|
|
NM_013987.3:c.529A=
|
NP_054642.2:p.Thr177=
|
|
NM_013988.3:c.172-227719A=
|
NP_054643.2:n.172-227719A=
|
|