ENST00000209873.9:c.1465G>T
MANE Select
|
ENSP00000209873.4:p.Ala489Ser
|
|
ENST00000546562.6:n.2529G>T
|
|
|
ENST00000547238.6:n.2101G>T
|
|
|
ENST00000547520.6:n.1581G>T
|
|
|
ENST00000547757.2:c.*383G>T
|
ENSP00000448020.2:n.*383G>T
|
|
ENST00000548880.2:n.1915G>T
|
|
|
ENST00000548931.6:c.900G>T
|
ENSP00000457518.1:p.Met300Ile
|
|
ENST00000549450.6:n.1399G>T
|
|
|
ENST00000552161.6:n.2543G>T
|
|
|
ENST00000672797.1:n.1954G>T
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|
|
ENST00000209873.8:c.1465G>T
|
ENSP00000209873.4:p.Ala489Ser
|
|
ENST00000394384.7:c.1366G>T
|
ENSP00000377908.3:p.Ala456Ser
|
|
ENST00000548931.5:c.900G>T
|
ENSP00000457518.1:p.Met300Ile
|
|
ENST00000550286.5:c.1093G>T
|
ENSP00000446885.1:p.Ala365Ser
|
|
ENST00000552876.5:n.1808G>T
|
|
|
NM_001173466.1:c.1366G>T
|
NP_001166937.1:p.Ala456Ser
|
|
NM_015665.5:c.1465G>T
|
NP_056480.1:p.Ala489Ser
|
|
XM_006719617.2:c.1480G>T
|
XP_006719680.1:p.Ala494Ser
|
|
XM_011538777.1:c.1522G>T
|
XP_011537079.1:p.Ala508Ser
|
|
XM_011538778.1:c.1507G>T
|
XP_011537080.1:p.Ala503Ser
|
|
XM_011538779.1:c.1423G>T
|
XP_011537081.1:p.Ala475Ser
|
|
XM_011538780.1:c.1408G>T
|
XP_011537082.1:p.Ala470Ser
|
|
XM_011538781.1:c.856G>T
|
XP_011537083.1:p.Ala286Ser
|
|
XM_011538778.2:c.1507G>T
|
XP_011537080.1:p.Ala503Ser
|
|
XM_011538780.2:c.1408G>T
|
XP_011537082.1:p.Ala470Ser
|
|
XR_001748875.2:n.1522G>T
|
|
|
NM_015665.6:c.1465G>T
MANE Select
|
NP_056480.1:p.Ala489Ser
|
|
NM_001173466.2:c.1366G>T
|
NP_001166937.1:p.Ala456Ser
|
|