ENST00000426263.10:c.702A>T
MANE Select
|
ENSP00000416293.2:p.Thr234=
|
|
ENST00000669445.1:c.57-25A>T
|
|
|
ENST00000674765.1:c.702A>T
|
ENSP00000501811.1:p.Thr234=
|
|
ENST00000675112.1:n.725A>T
|
|
|
ENST00000676254.1:n.1151A>T
|
|
|
ENST00000426263.7:c.702A>T
|
ENSP00000416293.2:p.Thr234=
|
|
ENST00000439722.2:c.581A>T
|
ENSP00000395521.2:n.581A>T
|
|
ENST00000475162.3:c.415+868A>T
|
|
|
ENST00000630287.2:c.*17A>T
|
ENSP00000486694.1:n.*17A>T
|
|
NM_006516.2:c.702A>T
|
NP_006507.2:p.Thr234=
|
|
NM_006516.3:c.702A>T
|
NP_006507.2:p.Thr234=
|
|
NM_006516.4:c.702A>T
MANE Select
|
NP_006507.2:p.Thr234=
|
|