ENST00000261304.7:c.247T>G
MANE Select
|
ENSP00000261304.2:p.Leu83Val
|
|
ENST00000261304.6:c.247T>G
|
ENSP00000261304.2:p.Leu83Val
|
|
ENST00000393568.8:c.196-265T>G
|
ENSP00000377198.4:n.196-265T>G
|
|
ENST00000393569.6:c.169T>G
|
ENSP00000377199.2:p.Leu57Val
|
|
ENST00000474294.6:n.237T>G
|
|
|
ENST00000544807.6:c.79T>G
|
ENSP00000437513.2:p.Leu27Val
|
|
ENST00000554372.5:c.247T>G
|
ENSP00000451884.1:p.Leu83Val
|
|
ENST00000554916.5:n.126T>G
|
|
|
ENST00000555956.1:n.52T>G
|
|
|
ENST00000556879.5:c.307T>G
|
ENSP00000452208.1:n.307T>G
|
|
ENST00000557316.5:c.247T>G
|
ENSP00000452314.1:p.Leu83Val
|
|
ENST00000622264.4:c.237T>G
|
|
|
NM_000153.3:c.247T>G
|
NP_000144.2:p.Leu83Val
|
|
NM_001201401.1:c.196-265T>G
|
NP_001188330.1:n.196-265T>G
|
|
NM_001201402.1:c.169T>G
|
NP_001188331.1:p.Leu57Val
|
|
XM_011536618.1:c.79T>G
|
XP_011534920.1:p.Leu27Val
|
|
XM_011536618.2:c.79T>G
|
XP_011534920.1:p.Leu27Val
|
|
NM_000153.4:c.247T>G
MANE Select
|
NP_000144.2:p.Leu83Val
|
|
NM_001201401.2:c.196-265T>G
|
NP_001188330.1:n.196-265T>G
|
|
NM_001201402.2:c.169T>G
|
NP_001188331.1:p.Leu57Val
|
|