ENST00000682424.1:c.628G>C
|
ENSP00000507321.1:p.Gly210Arg
|
|
ENST00000299427.12:c.742G>C
MANE Select
|
ENSP00000299427.6:p.Gly248Arg
|
|
ENST00000436873.7:c.312+496G>C
|
|
|
ENST00000524788.2:n.1901G>C
|
|
|
ENST00000524903.2:n.2017G>C
|
|
|
ENST00000528807.2:n.398G>C
|
|
|
ENST00000530040.2:n.480-302G>C
|
|
|
ENST00000533371.6:c.13G>C
|
ENSP00000437066.1:p.Gly5Arg
|
|
ENST00000642892.1:c.13G>C
|
ENSP00000494165.1:p.Gly5Arg
|
|
ENST00000643439.1:c.*482G>C
|
ENSP00000495849.1:n.*482G>C
|
|
ENST00000643479.1:n.771G>C
|
|
|
ENST00000643516.1:c.396-302G>C
|
|
|
ENST00000644151.1:n.2181G>C
|
|
|
ENST00000644218.1:c.742G>C
|
ENSP00000493574.1:p.Gly248Arg
|
|
ENST00000644683.1:c.*195G>C
|
ENSP00000494085.1:n.*195G>C
|
|
ENST00000644810.1:c.463G>C
|
ENSP00000495895.1:p.Gly155Arg
|
|
ENST00000644831.1:n.918G>C
|
|
|
ENST00000644933.1:c.13G>C
|
ENSP00000496133.1:p.Gly5Arg
|
|
ENST00000645020.1:n.2032G>C
|
|
|
ENST00000645285.1:c.13G>C
|
ENSP00000495058.1:p.Gly5Arg
|
|
ENST00000645331.1:n.1108G>C
|
|
|
ENST00000645620.1:c.13G>C
|
ENSP00000493657.1:p.Gly5Arg
|
|
ENST00000646777.1:n.918G>C
|
|
|
ENST00000647016.1:n.1222G>C
|
|
|
ENST00000647152.1:c.13G>C
|
ENSP00000495893.1:p.Gly5Arg
|
|
ENST00000647209.1:c.*611G>C
|
ENSP00000495558.1:n.*611G>C
|
|
ENST00000647346.1:n.1762G>C
|
|
|
ENST00000299427.10:c.742G>C
|
ENSP00000299427.6:p.Gly248Arg
|
|
ENST00000436873.6:c.451-302G>C
|
ENSP00000398136.2:n.451-302G>C
|
|
ENST00000524788.1:n.442G>C
|
|
|
ENST00000528807.1:n.292G>C
|
|
|
ENST00000533371.5:c.13G>C
|
ENSP00000437066.1:p.Gly5Arg
|
|
ENST00000611494.4:c.742G>C
|
ENSP00000484546.1:p.Gly248Arg
|
|
NM_000391.3:c.742G>C
|
NP_000382.3:p.Gly248Arg
|
|
NM_000391.4:c.742G>C
MANE Select
|
NP_000382.3:p.Gly248Arg
|
|