ENST00000465218.3:n.700T>C
|
|
|
ENST00000468748.7:n.660T>C
|
|
|
ENST00000484154.2:n.1298T>C
|
|
|
ENST00000491008.6:n.1425T>C
|
|
|
ENST00000492226.2:n.674T>C
|
|
|
ENST00000492773.6:c.409T>C
|
|
|
ENST00000647636.1:c.677T>C
|
ENSP00000497505.1:p.Phe226Ser
|
|
ENST00000647909.1:c.701T>C
|
ENSP00000498164.1:p.Phe234Ser
|
|
ENST00000648145.1:c.445T>C
|
|
|
ENST00000648189.1:c.427T>C
|
|
|
ENST00000648256.1:c.626T>C
|
ENSP00000497356.1:p.Phe209Ser
|
|
ENST00000648314.1:c.677T>C
|
ENSP00000496920.1:p.Phe226Ser
|
|
ENST00000648599.1:c.677T>C
|
ENSP00000497159.1:p.Phe226Ser
|
|
ENST00000648630.1:c.671T>C
|
ENSP00000497887.1:p.Phe224Ser
|
|
ENST00000648682.1:c.677T>C
|
ENSP00000498185.1:p.Phe226Ser
|
|
ENST00000648882.1:c.*503T>C
|
ENSP00000497603.1:n.*503T>C
|
|
ENST00000648890.1:c.677T>C
|
ENSP00000497503.1:p.Phe226Ser
|
|
ENST00000648915.2:c.677T>C
MANE Select
|
ENSP00000497160.1:p.Phe226Ser
|
|
ENST00000649545.1:c.411T>C
|
|
|
ENST00000649688.1:c.677T>C
|
ENSP00000497097.1:p.Phe226Ser
|
|
ENST00000649814.1:n.726T>C
|
|
|
ENST00000650270.1:c.544T>C
|
|
|
ENST00000273783.7:c.677T>C
|
ENSP00000273783.3:p.Phe226Ser
|
|
ENST00000432982.5:c.245+1393T>C
|
|
|
ENST00000444495.1:c.677T>C
|
ENSP00000409142.1:p.Phe226Ser
|
|
ENST00000468748.5:n.130T>C
|
|
|
ENST00000481054.5:n.678T>C
|
|
|
ENST00000491008.5:n.641T>C
|
|
|
ENST00000491144.5:n.1117T>C
|
|
|
NM_003907.2:c.677T>C
|
NP_003898.2:p.Phe226Ser
|
|
XR_924208.1:n.1628T>C
|
|
|
NM_003907.3:c.677T>C
MANE Select
|
NP_003898.2:p.Phe226Ser
|
|
XM_011513266.3:c.-225T>C
|
XP_011511568.1:n.-225T>C
|
|
XR_001740352.2:n.1040T>C
|
|
|
XR_001740353.2:n.1040T>C
|
|
|
XR_924208.2:n.1040T>C
|
|
|