ENST00000682424.1:c.*49G>C
|
ENSP00000507321.1:n.*49G>C
|
|
ENST00000299427.12:c.*49G>C
MANE Select
|
ENSP00000299427.6:n.*49G>C
|
|
ENST00000524611.2:n.780G>C
|
|
|
ENST00000533371.6:c.*49G>C
|
ENSP00000437066.1:n.*49G>C
|
|
ENST00000642892.1:c.*49G>C
|
ENSP00000494165.1:n.*49G>C
|
|
ENST00000643342.1:c.814G>C
|
|
|
ENST00000643439.1:c.*1481G>C
|
ENSP00000495849.1:n.*1481G>C
|
|
ENST00000643479.1:n.1927G>C
|
|
|
ENST00000643516.1:c.1250G>C
|
|
|
ENST00000644218.1:c.*49G>C
|
ENSP00000493574.1:n.*49G>C
|
|
ENST00000644683.1:c.*1194G>C
|
ENSP00000494085.1:n.*1194G>C
|
|
ENST00000644810.1:c.*49G>C
|
ENSP00000495895.1:n.*49G>C
|
|
ENST00000644831.1:n.1917G>C
|
|
|
ENST00000644933.1:c.*607G>C
|
ENSP00000496133.1:n.*607G>C
|
|
ENST00000645285.1:c.*607G>C
|
ENSP00000495058.1:n.*607G>C
|
|
ENST00000645331.1:n.2946G>C
|
|
|
ENST00000645620.1:c.*49G>C
|
ENSP00000493657.1:n.*49G>C
|
|
ENST00000646691.1:n.1628G>C
|
|
|
ENST00000646777.1:n.2074G>C
|
|
|
ENST00000647016.1:n.2221G>C
|
|
|
ENST00000647152.1:c.*49G>C
|
ENSP00000495893.1:n.*49G>C
|
|
ENST00000647209.1:c.*1610G>C
|
ENSP00000495558.1:n.*1610G>C
|
|
ENST00000647346.1:n.2761G>C
|
|
|
ENST00000299427.10:c.*49G>C
|
ENSP00000299427.6:n.*49G>C
|
|
ENST00000533371.5:c.*49G>C
|
ENSP00000437066.1:n.*49G>C
|
|
ENST00000611494.4:c.*69G>C
|
ENSP00000484546.1:n.*69G>C
|
|
NM_000391.3:c.*49G>C
|
NP_000382.3:n.*49G>C
|
|
NM_000391.4:c.*49G>C
MANE Select
|
NP_000382.3:n.*49G>C
|
|