ENST00000283871.10:c.391C>G
MANE Select
|
ENSP00000283871.5:p.Leu131Val
|
|
ENST00000283871.9:c.391C>G
|
ENSP00000283871.5:p.Leu131Val
|
|
ENST00000476082.2:c.268C>G
|
ENSP00000419560.2:p.Leu90Val
|
|
ENST00000485313.5:n.499C>G
|
|
|
ENST00000492108.5:c.22C>G
|
ENSP00000419838.1:p.Leu8Val
|
|
NM_000187.3:c.391C>G
|
NP_000178.2:p.Leu131Val
|
|
XM_005247412.1:c.391C>G
|
XP_005247469.1:p.Leu131Val
|
|
XM_005247413.1:c.391C>G
|
XP_005247470.1:p.Leu131Val
|
|
XM_005247414.3:c.391C>G
|
XP_005247471.1:p.Leu131Val
|
|
XM_011512746.1:c.391C>G
|
XP_011511048.1:p.Leu131Val
|
|
XM_005247412.2:c.391C>G
|
XP_005247469.1:p.Leu131Val
|
|
XM_005247413.2:c.391C>G
|
XP_005247470.1:p.Leu131Val
|
|
XM_005247414.5:c.391C>G
|
XP_005247471.1:p.Leu131Val
|
|
XM_011512746.2:c.391C>G
|
XP_011511048.1:p.Leu131Val
|
|
XM_017006277.2:c.-33C>G
|
XP_016861766.1:n.-33C>G
|
|
NM_000187.4:c.391C>G
MANE Select
|
NP_000178.2:p.Leu131Val
|
|