ENST00000299106.9:c.498C>T
MANE Select
|
ENSP00000299106.4:p.His166=
|
|
ENST00000299106.8:c.498C>T
|
ENSP00000299106.4:p.His166=
|
|
ENST00000441717.3:c.345C>T
|
ENSP00000395742.3:p.His115=
|
|
ENST00000524969.5:n.562C>T
|
|
|
ENST00000531302.5:n.497C>T
|
|
|
ENST00000532165.1:n.528C>T
|
|
|
ENST00000534549.5:c.318C>T
|
ENSP00000433206.1:p.His106=
|
|
NM_001205329.1:c.345C>T
|
NP_001192258.1:p.His115=
|
|
NM_032801.4:c.498C>T
|
NP_116190.3:p.His166=
|
|
NM_032801.5:c.498C>T
MANE Select
|
NP_116190.3:p.His166=
|
|
NM_001205329.2:c.345C>T
|
NP_001192258.1:p.His115=
|
|