ENST00000283871.10:c.249C>T
MANE Select
|
ENSP00000283871.5:p.His83=
|
|
ENST00000283871.9:c.249C>T
|
ENSP00000283871.5:p.His83=
|
|
ENST00000466528.5:n.275C>T
|
|
|
ENST00000476082.2:c.126C>T
|
ENSP00000419560.2:p.His42=
|
|
ENST00000485313.5:n.357C>T
|
|
|
ENST00000488183.5:n.507C>T
|
|
|
NM_000187.3:c.249C>T
|
NP_000178.2:p.His83=
|
|
XM_005247412.1:c.249C>T
|
XP_005247469.1:p.His83=
|
|
XM_005247413.1:c.249C>T
|
XP_005247470.1:p.His83=
|
|
XM_005247414.3:c.249C>T
|
XP_005247471.1:p.His83=
|
|
XM_011512746.1:c.249C>T
|
XP_011511048.1:p.His83=
|
|
XM_005247412.2:c.249C>T
|
XP_005247469.1:p.His83=
|
|
XM_005247413.2:c.249C>T
|
XP_005247470.1:p.His83=
|
|
XM_005247414.5:c.249C>T
|
XP_005247471.1:p.His83=
|
|
XM_011512746.2:c.249C>T
|
XP_011511048.1:p.His83=
|
|
XM_017006277.2:c.-175C>T
|
XP_016861766.1:n.-175C>T
|
|
NM_000187.4:c.249C>T
MANE Select
|
NP_000178.2:p.His83=
|
|