|
ENST00000700029.2:c.770T>C
|
ENSP00000514759.2:p.Phe257Ser
|
|
|
ENST00000710265.1:c.770T>C
|
ENSP00000518161.1:p.Phe257Ser
|
|
|
ENST00000472832.3:c.770T>C
|
ENSP00000483066.2:p.Phe257Ser
|
|
|
ENST00000688158.2:n.1505T>C
|
|
|
|
ENST00000688922.2:c.*600T>C
|
ENSP00000508742.2:n.*600T>C
|
|
|
ENST00000700021.1:c.725T>C
|
ENSP00000514757.1:p.Phe242Ser
|
|
|
ENST00000700022.1:c.*109T>C
|
ENSP00000514758.1:n.*109T>C
|
|
|
ENST00000700023.1:n.1928T>C
|
|
|
|
ENST00000700024.1:n.2162T>C
|
|
|
|
ENST00000700025.1:n.1539T>C
|
|
|
|
ENST00000700026.1:n.407T>C
|
|
|
|
ENST00000700029.1:c.604T>C
|
|
|
|
ENST00000706954.1:c.770T>C
|
ENSP00000516674.1:p.Phe257Ser
|
|
|
ENST00000706955.1:c.*805T>C
|
ENSP00000516675.1:n.*805T>C
|
|
|
ENST00000686459.1:c.*356T>C
|
ENSP00000508909.1:n.*356T>C
|
|
|
ENST00000688158.1:c.*881T>C
|
ENSP00000509254.1:n.*881T>C
|
|
|
ENST00000688308.1:c.770T>C
|
ENSP00000508752.1:p.Phe257Ser
|
|
|
ENST00000688922.1:c.691T>C
|
|
|
|
ENST00000693560.1:c.1289T>C
|
ENSP00000509861.1:p.Phe430Ser
|
|
|
ENST00000371953.8:c.770T>C
MANE Select
|
ENSP00000361021.3:p.Phe257Ser
|
|
|
ENST00000371953.7:c.770T>C
|
ENSP00000361021.3:p.Phe257Ser
|
|
|
ENST00000472832.2:c.197T>C
|
ENSP00000483066.1:p.Phe66Ser
|
|
|
NM_000314.5:c.770T>C
|
NP_000305.3:p.Phe257Ser
|
|
|
NM_000314.6:c.770T>C
|
NP_000305.3:p.Phe257Ser
|
|
|
NM_001304717.2:c.1289T>C
|
NP_001291646.2:p.Phe430Ser
|
|
|
NM_001304718.1:c.179T>C
|
NP_001291647.1:p.Phe60Ser
|
|
|
XM_006717926.2:c.725T>C
|
XP_006717989.1:p.Phe242Ser
|
|
|
XM_011539981.1:c.770T>C
|
XP_011538283.1:p.Phe257Ser
|
|
|
XM_011539982.1:c.674T>C
|
XP_011538284.1:p.Phe225Ser
|
|
|
XR_945791.1:n.1340T>C
|
|
|
|
NM_000314.7:c.770T>C
|
NP_000305.3:p.Phe257Ser
|
|
|
NM_001304717.5:c.1289T>C
|
NP_001291646.4:p.Phe430Ser
|
|
|
NM_001304718.2:c.179T>C
|
NP_001291647.1:p.Phe60Ser
|
|
|
NM_000314.8:c.770T>C
MANE Select
|
NP_000305.3:p.Phe257Ser
|
|
