ENST00000209873.9:c.1615C>G
MANE Select
|
ENSP00000209873.4:p.Pro539Ala
|
|
ENST00000546562.6:n.2679C>G
|
|
|
ENST00000547757.2:c.*533C>G
|
ENSP00000448020.2:n.*533C>G
|
|
ENST00000548931.6:c.1050C>G
|
ENSP00000457518.1:p.Cys350Trp
|
|
ENST00000549450.6:n.1549C>G
|
|
|
ENST00000209873.8:c.1615C>G
|
ENSP00000209873.4:p.Pro539Ala
|
|
ENST00000394384.7:c.1516C>G
|
ENSP00000377908.3:p.Pro506Ala
|
|
ENST00000548931.5:c.1050C>G
|
ENSP00000457518.1:p.Cys350Trp
|
|
ENST00000550286.5:c.1243C>G
|
ENSP00000446885.1:p.Pro415Ala
|
|
ENST00000552876.5:n.1958C>G
|
|
|
NM_001173466.1:c.1516C>G
|
NP_001166937.1:p.Pro506Ala
|
|
NM_015665.5:c.1615C>G
|
NP_056480.1:p.Pro539Ala
|
|
XM_006719617.2:c.1630C>G
|
XP_006719680.1:p.Pro544Ala
|
|
XM_011538777.1:c.1672C>G
|
XP_011537079.1:p.Pro558Ala
|
|
XM_011538778.1:c.1657C>G
|
XP_011537080.1:p.Pro553Ala
|
|
XM_011538779.1:c.1573C>G
|
XP_011537081.1:p.Pro525Ala
|
|
XM_011538780.1:c.1558C>G
|
XP_011537082.1:p.Pro520Ala
|
|
XM_011538781.1:c.1006C>G
|
XP_011537083.1:p.Pro336Ala
|
|
XM_011538778.2:c.1657C>G
|
XP_011537080.1:p.Pro553Ala
|
|
XM_011538780.2:c.1558C>G
|
XP_011537082.1:p.Pro520Ala
|
|
XR_001748875.2:n.1672C>G
|
|
|
NM_015665.6:c.1615C>G
MANE Select
|
NP_056480.1:p.Pro539Ala
|
|
NM_001173466.2:c.1516C>G
|
NP_001166937.1:p.Pro506Ala
|
|