ENST00000375731.9:c.666G>T
MANE Select
|
ENSP00000364883.5:p.Gln222His
|
|
ENST00000303617.5:c.579G>T
|
ENSP00000307334.5:p.Gln193His
|
|
ENST00000375731.8:c.666G>T
|
ENSP00000364883.4:p.Gln222His
|
|
NM_001306190.1:c.579G>T
|
NP_001293119.1:p.Gln193His
|
|
NM_001698.2:c.666G>T , LRG_449t1:c.666G>T
|
NP_001689.1:p.Gln222His
|
|
XM_005252066.2:c.696G>T
|
XP_005252123.1:p.Gln232His
|
|
XM_005252067.3:c.696G>T
|
XP_005252124.1:p.Gln232His
|
|
XM_005252069.3:c.696G>T
|
XP_005252126.1:p.Gln232His
|
|
XM_005252073.2:c.204G>T
|
XP_005252130.1:p.Gln68His
|
|
XM_006717150.2:c.609G>T
|
XP_006717213.1:p.Gln203His
|
|
XM_011518801.1:c.342G>T
|
XP_011517103.1:p.Gln114His
|
|
XM_011518802.1:c.339G>T
|
XP_011517104.1:p.Gln113His
|
|
NM_001351431.1:c.339G>T
|
NP_001338360.1:p.Gln113His
|
|
NM_001351432.1:c.339G>T
|
NP_001338361.1:p.Gln113His
|
|
NM_001351433.1:c.339G>T
|
NP_001338362.1:p.Gln113His
|
|
XM_005252066.3:c.696G>T
|
XP_005252123.1:p.Gln232His
|
|
XM_005252067.4:c.696G>T
|
XP_005252124.1:p.Gln232His
|
|
XM_005252069.4:c.696G>T
|
XP_005252126.1:p.Gln232His
|
|
XM_006717150.3:c.609G>T
|
XP_006717213.1:p.Gln203His
|
|
XM_017014849.1:c.666G>T
|
XP_016870338.1:p.Gln222His
|
|
XR_001746328.2:n.891G>T
|
|
|
XR_001746329.2:n.843G>T
|
|
|
NM_001698.3:c.666G>T
MANE Select
|
NP_001689.1:p.Gln222His
|
|
NM_001306190.2:c.579G>T
|
NP_001293119.1:p.Gln193His
|
|
NM_001351431.2:c.339G>T
|
NP_001338360.1:p.Gln113His
|
|
NM_001351432.2:c.339G>T
|
NP_001338361.1:p.Gln113His
|
|
NM_001351433.2:c.339G>T
|
NP_001338362.1:p.Gln113His
|
|