ENST00000400723.8:c.132C>T
MANE Select
|
ENSP00000383558.3:p.His44=
|
|
ENST00000400723.7:c.132C>T
|
ENSP00000383558.3:p.His44=
|
|
ENST00000570996.5:c.132C>T
|
ENSP00000460976.1:p.His44=
|
|
ENST00000572185.1:n.427C>T
|
|
|
ENST00000573428.1:c.132C>T
|
ENSP00000458930.1:p.His44=
|
|
ENST00000574283.2:n.66C>T
|
|
|
NM_000160.4:c.132C>T
|
NP_000151.1:p.His44=
|
|
XM_006722277.1:c.132C>T
|
XP_006722340.1:p.His44=
|
|
XM_011523539.1:c.-95C>T
|
XP_011521841.1:n.-95C>T
|
|
XM_011523540.1:c.-385C>T
|
XP_011521842.1:n.-385C>T
|
|
XM_017024446.1:c.126C>T
|
XP_016879935.1:p.His42=
|
|
XM_017024447.1:c.-385C>T
|
XP_016879936.1:n.-385C>T
|
|
NM_000160.5:c.132C>T
MANE Select
|
NP_000151.1:p.His44=
|
|