ENST00000426263.10:c.773C>T
MANE Select
|
ENSP00000416293.2:p.Thr258Ile
|
|
ENST00000669445.1:c.103C>T
|
|
|
ENST00000674765.1:c.773C>T
|
ENSP00000501811.1:p.Thr258Ile
|
|
ENST00000675112.1:n.796C>T
|
|
|
ENST00000676254.1:n.1222C>T
|
|
|
ENST00000426263.7:c.773C>T
|
ENSP00000416293.2:p.Thr258Ile
|
|
ENST00000439722.2:c.652C>T
|
ENSP00000395521.2:n.652C>T
|
|
ENST00000475162.3:c.415+939C>T
|
|
|
ENST00000630287.2:c.*88C>T
|
ENSP00000486694.1:n.*88C>T
|
|
NM_006516.2:c.773C>T
|
NP_006507.2:p.Thr258Ile
|
|
NM_006516.3:c.773C>T
|
NP_006507.2:p.Thr258Ile
|
|
NM_006516.4:c.773C>T
MANE Select
|
NP_006507.2:p.Thr258Ile
|
|