ENST00000209873.9:c.980T>G
MANE Select
|
ENSP00000209873.4:p.Leu327Arg
|
|
ENST00000546393.7:n.1825T>G
|
|
|
ENST00000546562.6:n.2044T>G
|
|
|
ENST00000547238.6:n.1616T>G
|
|
|
ENST00000547520.6:n.974T>G
|
|
|
ENST00000547757.2:c.29T>G
|
ENSP00000448020.2:p.Leu10Arg
|
|
ENST00000548880.2:n.1430T>G
|
|
|
ENST00000548931.6:c.500T>G
|
ENSP00000457518.1:p.Leu167Arg
|
|
ENST00000549450.6:n.914T>G
|
|
|
ENST00000552161.6:n.1936T>G
|
|
|
ENST00000672797.1:n.1433T>G
|
|
|
ENST00000672900.1:n.1778T>G
|
|
|
ENST00000209873.8:c.980T>G
|
ENSP00000209873.4:p.Leu327Arg
|
|
ENST00000394384.7:c.881T>G
|
ENSP00000377908.3:p.Leu294Arg
|
|
ENST00000546572.1:n.568T>G
|
|
|
ENST00000547520.5:n.684T>G
|
|
|
ENST00000548931.5:c.500T>G
|
ENSP00000457518.1:p.Leu167Arg
|
|
ENST00000550033.5:n.235T>G
|
|
|
ENST00000550286.5:c.608T>G
|
ENSP00000446885.1:p.Leu203Arg
|
|
ENST00000552876.5:n.1323T>G
|
|
|
NM_001173466.1:c.881T>G
|
NP_001166937.1:p.Leu294Arg
|
|
NM_015665.5:c.980T>G
|
NP_056480.1:p.Leu327Arg
|
|
XM_006719617.2:c.995T>G
|
XP_006719680.1:p.Leu332Arg
|
|
XM_006719619.2:c.995T>G
|
XP_006719682.1:p.Leu332Arg
|
|
XM_011538777.1:c.995T>G
|
XP_011537079.1:p.Leu332Arg
|
|
XM_011538778.1:c.980T>G
|
XP_011537080.1:p.Leu327Arg
|
|
XM_011538779.1:c.896T>G
|
XP_011537081.1:p.Leu299Arg
|
|
XM_011538780.1:c.881T>G
|
XP_011537082.1:p.Leu294Arg
|
|
XM_011538781.1:c.329T>G
|
XP_011537083.1:p.Leu110Arg
|
|
XM_011538778.2:c.980T>G
|
XP_011537080.1:p.Leu327Arg
|
|
XM_011538780.2:c.881T>G
|
XP_011537082.1:p.Leu294Arg
|
|
XR_001748875.2:n.1001T>G
|
|
|
NM_015665.6:c.980T>G
MANE Select
|
NP_056480.1:p.Leu327Arg
|
|
NM_001173466.2:c.881T>G
|
NP_001166937.1:p.Leu294Arg
|
|