ENST00000283871.10:c.639T>A
MANE Select
|
ENSP00000283871.5:p.Leu213=
|
|
ENST00000283871.9:c.639T>A
|
ENSP00000283871.5:p.Leu213=
|
|
ENST00000475447.2:c.170T>A
|
|
|
ENST00000492108.5:c.180+696T>A
|
ENSP00000419838.1:n.180+696T>A
|
|
ENST00000494453.1:c.59T>A
|
|
|
NM_000187.3:c.639T>A
|
NP_000178.2:p.Leu213=
|
|
XM_005247412.1:c.549+696T>A
|
XP_005247469.1:n.549+696T>A
|
|
XM_005247413.1:c.639T>A
|
XP_005247470.1:p.Leu213=
|
|
XM_005247414.3:c.639T>A
|
XP_005247471.1:p.Leu213=
|
|
XM_011512746.1:c.639T>A
|
XP_011511048.1:p.Leu213=
|
|
XM_005247412.2:c.549+696T>A
|
XP_005247469.1:n.549+696T>A
|
|
XM_005247413.2:c.639T>A
|
XP_005247470.1:p.Leu213=
|
|
XM_005247414.5:c.639T>A
|
XP_005247471.1:p.Leu213=
|
|
XM_011512746.2:c.639T>A
|
XP_011511048.1:p.Leu213=
|
|
XM_017006277.2:c.216T>A
|
XP_016861766.1:p.Leu72=
|
|
NM_000187.4:c.639T>A
MANE Select
|
NP_000178.2:p.Leu213=
|
|