ENST00000465218.3:n.684C>G
|
|
|
ENST00000468748.7:n.644C>G
|
|
|
ENST00000484154.2:n.1282C>G
|
|
|
ENST00000491008.6:n.1409C>G
|
|
|
ENST00000492226.2:n.658C>G
|
|
|
ENST00000492773.6:c.393C>G
|
|
|
ENST00000647636.1:c.661C>G
|
ENSP00000497505.1:p.Leu221Val
|
|
ENST00000647909.1:c.685C>G
|
ENSP00000498164.1:p.Leu229Val
|
|
ENST00000648145.1:c.429C>G
|
|
|
ENST00000648189.1:c.411C>G
|
|
|
ENST00000648256.1:c.610C>G
|
ENSP00000497356.1:p.Leu204Val
|
|
ENST00000648314.1:c.661C>G
|
ENSP00000496920.1:p.Leu221Val
|
|
ENST00000648599.1:c.661C>G
|
ENSP00000497159.1:p.Leu221Val
|
|
ENST00000648630.1:c.655C>G
|
ENSP00000497887.1:p.Leu219Val
|
|
ENST00000648682.1:c.661C>G
|
ENSP00000498185.1:p.Leu221Val
|
|
ENST00000648882.1:c.*487C>G
|
ENSP00000497603.1:n.*487C>G
|
|
ENST00000648890.1:c.661C>G
|
ENSP00000497503.1:p.Leu221Val
|
|
ENST00000648915.2:c.661C>G
MANE Select
|
ENSP00000497160.1:p.Leu221Val
|
|
ENST00000649545.1:c.395C>G
|
|
|
ENST00000649688.1:c.661C>G
|
ENSP00000497097.1:p.Leu221Val
|
|
ENST00000649814.1:n.710C>G
|
|
|
ENST00000650270.1:c.528C>G
|
|
|
ENST00000273783.7:c.661C>G
|
ENSP00000273783.3:p.Leu221Val
|
|
ENST00000432982.5:c.245+1377C>G
|
|
|
ENST00000444495.1:c.661C>G
|
ENSP00000409142.1:p.Leu221Val
|
|
ENST00000468748.5:n.114C>G
|
|
|
ENST00000481054.5:n.662C>G
|
|
|
ENST00000491008.5:n.625C>G
|
|
|
ENST00000491144.5:n.1101C>G
|
|
|
NM_003907.2:c.661C>G
|
NP_003898.2:p.Leu221Val
|
|
XR_924208.1:n.1612C>G
|
|
|
NM_003907.3:c.661C>G
MANE Select
|
NP_003898.2:p.Leu221Val
|
|
XM_011513266.3:c.-241C>G
|
XP_011511568.1:n.-241C>G
|
|
XR_001740352.2:n.1024C>G
|
|
|
XR_001740353.2:n.1024C>G
|
|
|
XR_924208.2:n.1024C>G
|
|
|