ENST00000209873.9:c.1427C>T
MANE Select
|
ENSP00000209873.4:p.Thr476Ile
|
|
ENST00000546562.6:n.2491C>T
|
|
|
ENST00000547238.6:n.2063C>T
|
|
|
ENST00000547520.6:n.1543C>T
|
|
|
ENST00000547757.2:c.*345C>T
|
ENSP00000448020.2:n.*345C>T
|
|
ENST00000548880.2:n.1877C>T
|
|
|
ENST00000548931.6:c.862C>T
|
ENSP00000457518.1:p.Gln288Ter
|
|
ENST00000549450.6:n.1361C>T
|
|
|
ENST00000552161.6:n.2505C>T
|
|
|
ENST00000672797.1:n.1916C>T
|
|
|
ENST00000209873.8:c.1427C>T
|
ENSP00000209873.4:p.Thr476Ile
|
|
ENST00000394384.7:c.1328C>T
|
ENSP00000377908.3:p.Thr443Ile
|
|
ENST00000548931.5:c.862C>T
|
ENSP00000457518.1:p.Gln288Ter
|
|
ENST00000550286.5:c.1055C>T
|
ENSP00000446885.1:p.Thr352Ile
|
|
ENST00000552876.5:n.1770C>T
|
|
|
NM_001173466.1:c.1328C>T
|
NP_001166937.1:p.Thr443Ile
|
|
NM_015665.5:c.1427C>T
|
NP_056480.1:p.Thr476Ile
|
|
XM_006719617.2:c.1442C>T
|
XP_006719680.1:p.Thr481Ile
|
|
XM_011538777.1:c.1484C>T
|
XP_011537079.1:p.Thr495Ile
|
|
XM_011538778.1:c.1469C>T
|
XP_011537080.1:p.Thr490Ile
|
|
XM_011538779.1:c.1385C>T
|
XP_011537081.1:p.Thr462Ile
|
|
XM_011538780.1:c.1370C>T
|
XP_011537082.1:p.Thr457Ile
|
|
XM_011538781.1:c.818C>T
|
XP_011537083.1:p.Thr273Ile
|
|
XM_011538778.2:c.1469C>T
|
XP_011537080.1:p.Thr490Ile
|
|
XM_011538780.2:c.1370C>T
|
XP_011537082.1:p.Thr457Ile
|
|
XR_001748875.2:n.1484C>T
|
|
|
NM_015665.6:c.1427C>T
MANE Select
|
NP_056480.1:p.Thr476Ile
|
|
NM_001173466.2:c.1328C>T
|
NP_001166937.1:p.Thr443Ile
|
|