ENST00000465218.3:n.535G>C
|
|
|
ENST00000468748.7:n.495G>C
|
|
|
ENST00000484154.2:n.1133G>C
|
|
|
ENST00000491008.6:n.1260G>C
|
|
|
ENST00000492226.2:n.509G>C
|
|
|
ENST00000492773.6:c.244G>C
|
|
|
ENST00000647636.1:c.512G>C
|
ENSP00000497505.1:p.Arg171Thr
|
|
ENST00000647909.1:c.536G>C
|
ENSP00000498164.1:p.Arg179Thr
|
|
ENST00000648145.1:c.280G>C
|
|
|
ENST00000648189.1:c.262G>C
|
|
|
ENST00000648256.1:c.461G>C
|
ENSP00000497356.1:p.Arg154Thr
|
|
ENST00000648314.1:c.512G>C
|
ENSP00000496920.1:p.Arg171Thr
|
|
ENST00000648599.1:c.512G>C
|
ENSP00000497159.1:p.Arg171Thr
|
|
ENST00000648630.1:c.506G>C
|
ENSP00000497887.1:p.Arg169Thr
|
|
ENST00000648682.1:c.512G>C
|
ENSP00000498185.1:p.Arg171Thr
|
|
ENST00000648882.1:c.*338G>C
|
ENSP00000497603.1:n.*338G>C
|
|
ENST00000648890.1:c.512G>C
|
ENSP00000497503.1:p.Arg171Thr
|
|
ENST00000648915.2:c.512G>C
MANE Select
|
ENSP00000497160.1:p.Arg171Thr
|
|
ENST00000649545.1:c.246G>C
|
|
|
ENST00000649688.1:c.512G>C
|
ENSP00000497097.1:p.Arg171Thr
|
|
ENST00000649814.1:n.561G>C
|
|
|
ENST00000650244.1:c.657G>C
|
ENSP00000497227.1:n.657G>C
|
|
ENST00000650270.1:c.379G>C
|
|
|
ENST00000273783.7:c.512G>C
|
ENSP00000273783.3:p.Arg171Thr
|
|
ENST00000432982.5:c.245+1228G>C
|
|
|
ENST00000444495.1:c.512G>C
|
ENSP00000409142.1:p.Arg171Thr
|
|
ENST00000481054.5:n.513G>C
|
|
|
ENST00000491008.5:n.476G>C
|
|
|
ENST00000491144.5:n.952G>C
|
|
|
ENST00000498831.1:n.467G>C
|
|
|
NM_003907.2:c.512G>C
|
NP_003898.2:p.Arg171Thr
|
|
XR_924208.1:n.1463G>C
|
|
|
NM_003907.3:c.512G>C
MANE Select
|
NP_003898.2:p.Arg171Thr
|
|
XM_011513266.3:c.-390G>C
|
XP_011511568.1:n.-390G>C
|
|
XR_001740352.2:n.875G>C
|
|
|
XR_001740353.2:n.875G>C
|
|
|
XR_924208.2:n.875G>C
|
|
|