ENST00000209873.9:c.1588C>A
MANE Select
|
ENSP00000209873.4:p.Pro530Thr
|
|
ENST00000546562.6:n.2652C>A
|
|
|
ENST00000547238.6:n.2224C>A
|
|
|
ENST00000547520.6:n.1704C>A
|
|
|
ENST00000547757.2:c.*506C>A
|
ENSP00000448020.2:n.*506C>A
|
|
ENST00000548931.6:c.1023C>A
|
ENSP00000457518.1:p.Thr341=
|
|
ENST00000549450.6:n.1522C>A
|
|
|
ENST00000672797.1:n.2077C>A
|
|
|
ENST00000209873.8:c.1588C>A
|
ENSP00000209873.4:p.Pro530Thr
|
|
ENST00000394384.7:c.1489C>A
|
ENSP00000377908.3:p.Pro497Thr
|
|
ENST00000548931.5:c.1023C>A
|
ENSP00000457518.1:p.Thr341=
|
|
ENST00000550286.5:c.1216C>A
|
ENSP00000446885.1:p.Pro406Thr
|
|
ENST00000552876.5:n.1931C>A
|
|
|
NM_001173466.1:c.1489C>A
|
NP_001166937.1:p.Pro497Thr
|
|
NM_015665.5:c.1588C>A
|
NP_056480.1:p.Pro530Thr
|
|
XM_006719617.2:c.1603C>A
|
XP_006719680.1:p.Pro535Thr
|
|
XM_011538777.1:c.1645C>A
|
XP_011537079.1:p.Pro549Thr
|
|
XM_011538778.1:c.1630C>A
|
XP_011537080.1:p.Pro544Thr
|
|
XM_011538779.1:c.1546C>A
|
XP_011537081.1:p.Pro516Thr
|
|
XM_011538780.1:c.1531C>A
|
XP_011537082.1:p.Pro511Thr
|
|
XM_011538781.1:c.979C>A
|
XP_011537083.1:p.Pro327Thr
|
|
XM_011538778.2:c.1630C>A
|
XP_011537080.1:p.Pro544Thr
|
|
XM_011538780.2:c.1531C>A
|
XP_011537082.1:p.Pro511Thr
|
|
XR_001748875.2:n.1645C>A
|
|
|
NM_015665.6:c.1588C>A
MANE Select
|
NP_056480.1:p.Pro530Thr
|
|
NM_001173466.2:c.1489C>A
|
NP_001166937.1:p.Pro497Thr
|
|