ENST00000696264.1:c.517C>G
|
ENSP00000512511.1:p.Leu173Val
|
|
ENST00000696265.1:c.517C>G
|
ENSP00000512512.1:p.Leu173Val
|
|
ENST00000696266.1:c.235C>G
|
ENSP00000512513.1:p.Leu79Val
|
|
ENST00000696267.1:n.157C>G
|
|
|
ENST00000229769.3:c.517C>G
MANE Select
|
ENSP00000229769.2:p.Leu173Val
|
|
ENST00000648059.1:c.517C>G
|
ENSP00000497902.1:p.Leu173Val
|
|
ENST00000229769.2:c.517C>G
|
ENSP00000229769.2:p.Leu173Val
|
|
NM_021922.2:c.517C>G , LRG_498t1:c.517C>G
|
NP_068741.1:p.Leu173Val
|
|
XM_005248885.2:c.517C>G
|
XP_005248942.1:p.Leu173Val
|
|
XM_005248886.2:c.517C>G
|
XP_005248943.1:p.Leu173Val
|
|
XM_005248887.2:c.517C>G
|
XP_005248944.1:p.Leu173Val
|
|
XM_005248888.2:c.517C>G
|
XP_005248945.1:p.Leu173Val
|
|
XM_011514343.1:c.223C>G
|
XP_011512645.1:p.Leu75Val
|
|
XM_011514344.1:c.223C>G
|
XP_011512646.1:p.Leu75Val
|
|
XM_005248888.3:c.517C>G
|
XP_005248945.1:p.Leu173Val
|
|
XM_011514343.2:c.223C>G
|
XP_011512645.1:p.Leu75Val
|
|
XR_001743226.1:n.724C>G
|
|
|
XR_002956267.1:n.724C>G
|
|
|
NM_021922.3:c.517C>G
MANE Select
|
NP_068741.1:p.Leu173Val
|
|