ENST00000217958.8:c.529C>T
MANE Select
|
ENSP00000217958.3:p.His177Tyr
|
|
ENST00000217958.7:c.529C>T
|
ENSP00000217958.3:p.His177Tyr
|
|
ENST00000340200.5:c.430C>T
|
ENSP00000345963.5:p.His144Tyr
|
|
ENST00000361815.9:c.450C>T
|
ENSP00000354906.5:p.Asp150=
|
|
ENST00000372295.5:c.406C>T
|
ENSP00000361369.1:p.His136Tyr
|
|
ENST00000372296.5:c.327C>T
|
ENSP00000361370.1:p.Asp109=
|
|
NM_002814.3:c.529C>T
|
NP_002805.1:p.His177Tyr
|
|
NM_170750.2:c.450C>T
|
NP_736606.1:p.Asp150=
|
|
NM_002814.4:c.529C>T
MANE Select
|
NP_002805.1:p.His177Tyr
|
|
NM_170750.3:c.450C>T
|
NP_736606.1:p.Asp150=
|
|