ENST00000465218.3:n.676C>G
|
|
|
ENST00000468748.7:n.636C>G
|
|
|
ENST00000484154.2:n.1274C>G
|
|
|
ENST00000491008.6:n.1401C>G
|
|
|
ENST00000492226.2:n.650C>G
|
|
|
ENST00000492773.6:c.385C>G
|
|
|
ENST00000647636.1:c.653C>G
|
ENSP00000497505.1:p.Thr218Ser
|
|
ENST00000647909.1:c.677C>G
|
ENSP00000498164.1:p.Thr226Ser
|
|
ENST00000648145.1:c.421C>G
|
|
|
ENST00000648189.1:c.403C>G
|
|
|
ENST00000648256.1:c.602C>G
|
ENSP00000497356.1:p.Thr201Ser
|
|
ENST00000648314.1:c.653C>G
|
ENSP00000496920.1:p.Thr218Ser
|
|
ENST00000648599.1:c.653C>G
|
ENSP00000497159.1:p.Thr218Ser
|
|
ENST00000648630.1:c.647C>G
|
ENSP00000497887.1:p.Thr216Ser
|
|
ENST00000648682.1:c.653C>G
|
ENSP00000498185.1:p.Thr218Ser
|
|
ENST00000648882.1:c.*479C>G
|
ENSP00000497603.1:n.*479C>G
|
|
ENST00000648890.1:c.653C>G
|
ENSP00000497503.1:p.Thr218Ser
|
|
ENST00000648915.2:c.653C>G
MANE Select
|
ENSP00000497160.1:p.Thr218Ser
|
|
ENST00000649545.1:c.387C>G
|
|
|
ENST00000649688.1:c.653C>G
|
ENSP00000497097.1:p.Thr218Ser
|
|
ENST00000649814.1:n.702C>G
|
|
|
ENST00000650270.1:c.520C>G
|
|
|
ENST00000273783.7:c.653C>G
|
ENSP00000273783.3:p.Thr218Ser
|
|
ENST00000432982.5:c.245+1369C>G
|
|
|
ENST00000444495.1:c.653C>G
|
ENSP00000409142.1:p.Thr218Ser
|
|
ENST00000468748.5:n.106C>G
|
|
|
ENST00000481054.5:n.654C>G
|
|
|
ENST00000491008.5:n.617C>G
|
|
|
ENST00000491144.5:n.1093C>G
|
|
|
NM_003907.2:c.653C>G
|
NP_003898.2:p.Thr218Ser
|
|
XR_924208.1:n.1604C>G
|
|
|
NM_003907.3:c.653C>G
MANE Select
|
NP_003898.2:p.Thr218Ser
|
|
XM_011513266.3:c.-249C>G
|
XP_011511568.1:n.-249C>G
|
|
XR_001740352.2:n.1016C>G
|
|
|
XR_001740353.2:n.1016C>G
|
|
|
XR_924208.2:n.1016C>G
|
|
|