ENST00000682568.1:n.1821T=
|
|
|
ENST00000682617.1:c.1881T=
|
ENSP00000507912.1:p.Tyr627=
|
|
ENST00000682826.1:c.*1057T=
|
ENSP00000507274.1:n.*1057T=
|
|
ENST00000682909.1:n.3783T=
|
|
|
ENST00000683277.1:n.3388T=
|
|
|
ENST00000683407.1:n.1751T=
|
|
|
ENST00000683962.1:c.*1437T=
|
ENSP00000506854.1:n.*1437T=
|
|
ENST00000311895.8:c.1743T=
MANE Select
|
ENSP00000310520.7:p.Tyr581=
|
|
ENST00000311895.7:c.1743T=
|
ENSP00000310520.7:p.Tyr581=
|
|
ENST00000389138.7:n.1020T=
|
|
|
NM_005236.2:c.1743T= , LRG_463t1:c.1743T=
|
NP_005227.1:p.Tyr581=
|
|
XM_011522424.1:c.1881T=
|
XP_011520726.1:p.Tyr627=
|
|
XM_011522425.1:c.1200T=
|
XP_011520727.1:p.Tyr400=
|
|
XM_011522426.1:c.954T=
|
XP_011520728.1:p.Tyr318=
|
|
XM_011522427.1:c.393T=
|
XP_011520729.1:p.Tyr131=
|
|
XR_932805.1:n.1902T=
|
|
|
XM_011522424.3:c.1881T=
|
XP_011520726.1:p.Tyr627=
|
|
XM_017023043.2:c.954T=
|
XP_016878532.1:p.Tyr318=
|
|
NM_005236.3:c.1743T=
MANE Select
|
NP_005227.1:p.Tyr581=
|
|