ENST00000209873.9:c.1458T>C
MANE Select
|
ENSP00000209873.4:p.Phe486=
|
|
ENST00000546562.6:n.2522T>C
|
|
|
ENST00000547238.6:n.2094T>C
|
|
|
ENST00000547520.6:n.1574T>C
|
|
|
ENST00000547757.2:c.*376T>C
|
ENSP00000448020.2:n.*376T>C
|
|
ENST00000548880.2:n.1908T>C
|
|
|
ENST00000548931.6:c.893T>C
|
ENSP00000457518.1:p.Leu298Ser
|
|
ENST00000549450.6:n.1392T>C
|
|
|
ENST00000552161.6:n.2536T>C
|
|
|
ENST00000672797.1:n.1947T>C
|
|
|
ENST00000209873.8:c.1458T>C
|
ENSP00000209873.4:p.Phe486=
|
|
ENST00000394384.7:c.1359T>C
|
ENSP00000377908.3:p.Phe453=
|
|
ENST00000548931.5:c.893T>C
|
ENSP00000457518.1:p.Leu298Ser
|
|
ENST00000550286.5:c.1086T>C
|
ENSP00000446885.1:p.Phe362=
|
|
ENST00000552876.5:n.1801T>C
|
|
|
NM_001173466.1:c.1359T>C
|
NP_001166937.1:p.Phe453=
|
|
NM_015665.5:c.1458T>C
|
NP_056480.1:p.Phe486=
|
|
XM_006719617.2:c.1473T>C
|
XP_006719680.1:p.Phe491=
|
|
XM_011538777.1:c.1515T>C
|
XP_011537079.1:p.Phe505=
|
|
XM_011538778.1:c.1500T>C
|
XP_011537080.1:p.Phe500=
|
|
XM_011538779.1:c.1416T>C
|
XP_011537081.1:p.Phe472=
|
|
XM_011538780.1:c.1401T>C
|
XP_011537082.1:p.Phe467=
|
|
XM_011538781.1:c.849T>C
|
XP_011537083.1:p.Phe283=
|
|
XM_011538778.2:c.1500T>C
|
XP_011537080.1:p.Phe500=
|
|
XM_011538780.2:c.1401T>C
|
XP_011537082.1:p.Phe467=
|
|
XR_001748875.2:n.1515T>C
|
|
|
NM_015665.6:c.1458T>C
MANE Select
|
NP_056480.1:p.Phe486=
|
|
NM_001173466.2:c.1359T>C
|
NP_001166937.1:p.Phe453=
|
|