ENST00000399391.7:c.474C>T
|
ENSP00000382323.2:p.His158=
|
|
ENST00000399397.6:c.438C>T
MANE Select
|
ENSP00000382329.2:p.His146=
|
|
ENST00000399391.6:c.474C>T
|
ENSP00000382323.2:p.His158=
|
|
ENST00000399397.5:c.438C>T
|
ENSP00000382329.2:p.His146=
|
|
ENST00000428619.1:c.255C>T
|
ENSP00000399057.2:p.His85=
|
|
ENST00000498332.5:n.344C>T
|
|
|
NM_001277269.1:c.474C>T
|
NP_001264198.1:p.His158=
|
|
NM_001292063.1:c.438C>T
|
NP_001278992.1:p.His146=
|
|
NM_001277269.2:c.474C>T
|
NP_001264198.1:p.His158=
|
|
NM_001292063.2:c.438C>T
MANE Select
|
NP_001278992.1:p.His146=
|
|