ENST00000283871.10:c.183G>C
MANE Select
|
ENSP00000283871.5:p.Leu61=
|
|
ENST00000283871.9:c.183G>C
|
ENSP00000283871.5:p.Leu61=
|
|
ENST00000466528.5:n.209G>C
|
|
|
ENST00000476082.2:c.60G>C
|
ENSP00000419560.2:p.Leu20=
|
|
ENST00000485313.5:n.291G>C
|
|
|
ENST00000488183.5:n.441G>C
|
|
|
NM_000187.3:c.183G>C
|
NP_000178.2:p.Leu61=
|
|
XM_005247412.1:c.183G>C
|
XP_005247469.1:p.Leu61=
|
|
XM_005247413.1:c.183G>C
|
XP_005247470.1:p.Leu61=
|
|
XM_005247414.3:c.183G>C
|
XP_005247471.1:p.Leu61=
|
|
XM_011512746.1:c.183G>C
|
XP_011511048.1:p.Leu61=
|
|
XM_005247412.2:c.183G>C
|
XP_005247469.1:p.Leu61=
|
|
XM_005247413.2:c.183G>C
|
XP_005247470.1:p.Leu61=
|
|
XM_005247414.5:c.183G>C
|
XP_005247471.1:p.Leu61=
|
|
XM_011512746.2:c.183G>C
|
XP_011511048.1:p.Leu61=
|
|
XM_017006277.2:c.-241G>C
|
XP_016861766.1:n.-241G>C
|
|
NM_000187.4:c.183G>C
MANE Select
|
NP_000178.2:p.Leu61=
|
|