ENST00000209873.9:c.1588C>G
MANE Select
|
ENSP00000209873.4:p.Pro530Ala
|
|
ENST00000546562.6:n.2652C>G
|
|
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ENST00000547238.6:n.2224C>G
|
|
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ENST00000547520.6:n.1704C>G
|
|
|
ENST00000547757.2:c.*506C>G
|
ENSP00000448020.2:n.*506C>G
|
|
ENST00000548931.6:c.1023C>G
|
ENSP00000457518.1:p.Thr341=
|
|
ENST00000549450.6:n.1522C>G
|
|
|
ENST00000672797.1:n.2077C>G
|
|
|
ENST00000209873.8:c.1588C>G
|
ENSP00000209873.4:p.Pro530Ala
|
|
ENST00000394384.7:c.1489C>G
|
ENSP00000377908.3:p.Pro497Ala
|
|
ENST00000548931.5:c.1023C>G
|
ENSP00000457518.1:p.Thr341=
|
|
ENST00000550286.5:c.1216C>G
|
ENSP00000446885.1:p.Pro406Ala
|
|
ENST00000552876.5:n.1931C>G
|
|
|
NM_001173466.1:c.1489C>G
|
NP_001166937.1:p.Pro497Ala
|
|
NM_015665.5:c.1588C>G
|
NP_056480.1:p.Pro530Ala
|
|
XM_006719617.2:c.1603C>G
|
XP_006719680.1:p.Pro535Ala
|
|
XM_011538777.1:c.1645C>G
|
XP_011537079.1:p.Pro549Ala
|
|
XM_011538778.1:c.1630C>G
|
XP_011537080.1:p.Pro544Ala
|
|
XM_011538779.1:c.1546C>G
|
XP_011537081.1:p.Pro516Ala
|
|
XM_011538780.1:c.1531C>G
|
XP_011537082.1:p.Pro511Ala
|
|
XM_011538781.1:c.979C>G
|
XP_011537083.1:p.Pro327Ala
|
|
XM_011538778.2:c.1630C>G
|
XP_011537080.1:p.Pro544Ala
|
|
XM_011538780.2:c.1531C>G
|
XP_011537082.1:p.Pro511Ala
|
|
XR_001748875.2:n.1645C>G
|
|
|
NM_015665.6:c.1588C>G
MANE Select
|
NP_056480.1:p.Pro530Ala
|
|
NM_001173466.2:c.1489C>G
|
NP_001166937.1:p.Pro497Ala
|
|