ENST00000283871.10:c.835C>G
MANE Select
|
ENSP00000283871.5:p.Leu279Val
|
|
ENST00000283871.9:c.835C>G
|
ENSP00000283871.5:p.Leu279Val
|
|
ENST00000470321.1:n.175C>G
|
|
|
ENST00000475447.2:c.263C>G
|
|
|
ENST00000492108.5:c.241C>G
|
ENSP00000419838.1:p.Leu81Val
|
|
ENST00000494453.1:c.255C>G
|
|
|
NM_000187.3:c.835C>G
|
NP_000178.2:p.Leu279Val
|
|
XM_005247412.1:c.610C>G
|
XP_005247469.1:p.Leu204Val
|
|
XM_005247413.1:c.835C>G
|
XP_005247470.1:p.Leu279Val
|
|
XM_011512746.1:c.835C>G
|
XP_011511048.1:p.Leu279Val
|
|
XM_005247412.2:c.610C>G
|
XP_005247469.1:p.Leu204Val
|
|
XM_005247413.2:c.835C>G
|
XP_005247470.1:p.Leu279Val
|
|
XM_011512746.2:c.835C>G
|
XP_011511048.1:p.Leu279Val
|
|
XM_017006277.2:c.412C>G
|
XP_016861766.1:p.Leu138Val
|
|
NM_000187.4:c.835C>G
MANE Select
|
NP_000178.2:p.Leu279Val
|
|