ENST00000375731.9:c.833T>G
MANE Select
|
ENSP00000364883.5:p.Phe278Cys
|
|
ENST00000303617.5:c.746T>G
|
ENSP00000307334.5:p.Phe249Cys
|
|
ENST00000375731.8:c.833T>G
|
ENSP00000364883.4:p.Phe278Cys
|
|
ENST00000473695.1:n.105T>G
|
|
|
NM_001306190.1:c.746T>G
|
NP_001293119.1:p.Phe249Cys
|
|
NM_001698.2:c.833T>G , LRG_449t1:c.833T>G
|
NP_001689.1:p.Phe278Cys
|
|
XM_005252066.2:c.863T>G
|
XP_005252123.1:p.Phe288Cys
|
|
XM_005252067.3:c.863T>G
|
XP_005252124.1:p.Phe288Cys
|
|
XM_005252069.3:c.863T>G
|
XP_005252126.1:p.Phe288Cys
|
|
XM_005252073.2:c.371T>G
|
XP_005252130.1:p.Phe124Cys
|
|
XM_006717150.2:c.776T>G
|
XP_006717213.1:p.Phe259Cys
|
|
XM_011518801.1:c.509T>G
|
XP_011517103.1:p.Phe170Cys
|
|
XM_011518802.1:c.506T>G
|
XP_011517104.1:p.Phe169Cys
|
|
NM_001351431.1:c.506T>G
|
NP_001338360.1:p.Phe169Cys
|
|
NM_001351432.1:c.506T>G
|
NP_001338361.1:p.Phe169Cys
|
|
NM_001351433.1:c.506T>G
|
NP_001338362.1:p.Phe169Cys
|
|
XM_005252066.3:c.863T>G
|
XP_005252123.1:p.Phe288Cys
|
|
XM_005252067.4:c.863T>G
|
XP_005252124.1:p.Phe288Cys
|
|
XM_005252069.4:c.863T>G
|
XP_005252126.1:p.Phe288Cys
|
|
XM_006717150.3:c.776T>G
|
XP_006717213.1:p.Phe259Cys
|
|
XM_017014849.1:c.833T>G
|
XP_016870338.1:p.Phe278Cys
|
|
XR_001746328.2:n.1058T>G
|
|
|
XR_001746329.2:n.1010T>G
|
|
|
NM_001698.3:c.833T>G
MANE Select
|
NP_001689.1:p.Phe278Cys
|
|
NM_001306190.2:c.746T>G
|
NP_001293119.1:p.Phe249Cys
|
|
NM_001351431.2:c.506T>G
|
NP_001338360.1:p.Phe169Cys
|
|
NM_001351432.2:c.506T>G
|
NP_001338361.1:p.Phe169Cys
|
|
NM_001351433.2:c.506T>G
|
NP_001338362.1:p.Phe169Cys
|
|