ENST00000375731.9:c.694C>G
MANE Select
|
ENSP00000364883.5:p.Leu232Val
|
|
ENST00000303617.5:c.607C>G
|
ENSP00000307334.5:p.Leu203Val
|
|
ENST00000375731.8:c.694C>G
|
ENSP00000364883.4:p.Leu232Val
|
|
NM_001306190.1:c.607C>G
|
NP_001293119.1:p.Leu203Val
|
|
NM_001698.2:c.694C>G , LRG_449t1:c.694C>G
|
NP_001689.1:p.Leu232Val
|
|
XM_005252066.2:c.724C>G
|
XP_005252123.1:p.Leu242Val
|
|
XM_005252067.3:c.724C>G
|
XP_005252124.1:p.Leu242Val
|
|
XM_005252069.3:c.724C>G
|
XP_005252126.1:p.Leu242Val
|
|
XM_005252073.2:c.232C>G
|
XP_005252130.1:p.Leu78Val
|
|
XM_006717150.2:c.637C>G
|
XP_006717213.1:p.Leu213Val
|
|
XM_011518801.1:c.370C>G
|
XP_011517103.1:p.Leu124Val
|
|
XM_011518802.1:c.367C>G
|
XP_011517104.1:p.Leu123Val
|
|
NM_001351431.1:c.367C>G
|
NP_001338360.1:p.Leu123Val
|
|
NM_001351432.1:c.367C>G
|
NP_001338361.1:p.Leu123Val
|
|
NM_001351433.1:c.367C>G
|
NP_001338362.1:p.Leu123Val
|
|
XM_005252066.3:c.724C>G
|
XP_005252123.1:p.Leu242Val
|
|
XM_005252067.4:c.724C>G
|
XP_005252124.1:p.Leu242Val
|
|
XM_005252069.4:c.724C>G
|
XP_005252126.1:p.Leu242Val
|
|
XM_006717150.3:c.637C>G
|
XP_006717213.1:p.Leu213Val
|
|
XM_017014849.1:c.694C>G
|
XP_016870338.1:p.Leu232Val
|
|
XR_001746328.2:n.919C>G
|
|
|
XR_001746329.2:n.871C>G
|
|
|
NM_001698.3:c.694C>G
MANE Select
|
NP_001689.1:p.Leu232Val
|
|
NM_001306190.2:c.607C>G
|
NP_001293119.1:p.Leu203Val
|
|
NM_001351431.2:c.367C>G
|
NP_001338360.1:p.Leu123Val
|
|
NM_001351432.2:c.367C>G
|
NP_001338361.1:p.Leu123Val
|
|
NM_001351433.2:c.367C>G
|
NP_001338362.1:p.Leu123Val
|
|