ENST00000209873.9:c.1553T>A
MANE Select
|
ENSP00000209873.4:p.Phe518Tyr
|
|
ENST00000546562.6:n.2617T>A
|
|
|
ENST00000547238.6:n.2189T>A
|
|
|
ENST00000547520.6:n.1669T>A
|
|
|
ENST00000547757.2:c.*471T>A
|
ENSP00000448020.2:n.*471T>A
|
|
ENST00000548931.6:c.988T>A
|
ENSP00000457518.1:p.Leu330Ile
|
|
ENST00000549450.6:n.1487T>A
|
|
|
ENST00000672797.1:n.2042T>A
|
|
|
ENST00000209873.8:c.1553T>A
|
ENSP00000209873.4:p.Phe518Tyr
|
|
ENST00000394384.7:c.1454T>A
|
ENSP00000377908.3:p.Phe485Tyr
|
|
ENST00000548931.5:c.988T>A
|
ENSP00000457518.1:p.Leu330Ile
|
|
ENST00000550286.5:c.1181T>A
|
ENSP00000446885.1:p.Phe394Tyr
|
|
ENST00000552876.5:n.1896T>A
|
|
|
NM_001173466.1:c.1454T>A
|
NP_001166937.1:p.Phe485Tyr
|
|
NM_015665.5:c.1553T>A
|
NP_056480.1:p.Phe518Tyr
|
|
XM_006719617.2:c.1568T>A
|
XP_006719680.1:p.Phe523Tyr
|
|
XM_011538777.1:c.1610T>A
|
XP_011537079.1:p.Phe537Tyr
|
|
XM_011538778.1:c.1595T>A
|
XP_011537080.1:p.Phe532Tyr
|
|
XM_011538779.1:c.1511T>A
|
XP_011537081.1:p.Phe504Tyr
|
|
XM_011538780.1:c.1496T>A
|
XP_011537082.1:p.Phe499Tyr
|
|
XM_011538781.1:c.944T>A
|
XP_011537083.1:p.Phe315Tyr
|
|
XM_011538778.2:c.1595T>A
|
XP_011537080.1:p.Phe532Tyr
|
|
XM_011538780.2:c.1496T>A
|
XP_011537082.1:p.Phe499Tyr
|
|
XR_001748875.2:n.1610T>A
|
|
|
NM_015665.6:c.1553T>A
MANE Select
|
NP_056480.1:p.Phe518Tyr
|
|
NM_001173466.2:c.1454T>A
|
NP_001166937.1:p.Phe485Tyr
|
|