ENST00000217958.8:c.531C>T
MANE Select
|
ENSP00000217958.3:p.His177=
|
|
ENST00000217958.7:c.531C>T
|
ENSP00000217958.3:p.His177=
|
|
ENST00000340200.5:c.432C>T
|
ENSP00000345963.5:p.His144=
|
|
ENST00000361815.9:c.452C>T
|
ENSP00000354906.5:p.Thr151Ile
|
|
ENST00000372295.5:c.408C>T
|
ENSP00000361369.1:p.His136=
|
|
ENST00000372296.5:c.329C>T
|
ENSP00000361370.1:p.Thr110Ile
|
|
NM_002814.3:c.531C>T
|
NP_002805.1:p.His177=
|
|
NM_170750.2:c.452C>T
|
NP_736606.1:p.Thr151Ile
|
|
NM_002814.4:c.531C>T
MANE Select
|
NP_002805.1:p.His177=
|
|
NM_170750.3:c.452C>T
|
NP_736606.1:p.Thr151Ile
|
|