ENST00000682424.1:c.*17G>C
|
ENSP00000507321.1:n.*17G>C
|
|
ENST00000299427.12:c.*17G>C
MANE Select
|
ENSP00000299427.6:n.*17G>C
|
|
ENST00000524611.2:n.748G>C
|
|
|
ENST00000533371.6:c.*17G>C
|
ENSP00000437066.1:n.*17G>C
|
|
ENST00000642892.1:c.*17G>C
|
ENSP00000494165.1:n.*17G>C
|
|
ENST00000643342.1:c.782G>C
|
|
|
ENST00000643439.1:c.*1449G>C
|
ENSP00000495849.1:n.*1449G>C
|
|
ENST00000643479.1:n.1895G>C
|
|
|
ENST00000643516.1:c.1218G>C
|
|
|
ENST00000644218.1:c.*17G>C
|
ENSP00000493574.1:n.*17G>C
|
|
ENST00000644683.1:c.*1162G>C
|
ENSP00000494085.1:n.*1162G>C
|
|
ENST00000644810.1:c.*17G>C
|
ENSP00000495895.1:n.*17G>C
|
|
ENST00000644831.1:n.1885G>C
|
|
|
ENST00000644933.1:c.*575G>C
|
ENSP00000496133.1:n.*575G>C
|
|
ENST00000645285.1:c.*575G>C
|
ENSP00000495058.1:n.*575G>C
|
|
ENST00000645331.1:n.2914G>C
|
|
|
ENST00000645620.1:c.*17G>C
|
ENSP00000493657.1:n.*17G>C
|
|
ENST00000646691.1:n.1596G>C
|
|
|
ENST00000646777.1:n.2042G>C
|
|
|
ENST00000647016.1:n.2189G>C
|
|
|
ENST00000647152.1:c.*17G>C
|
ENSP00000495893.1:n.*17G>C
|
|
ENST00000647209.1:c.*1578G>C
|
ENSP00000495558.1:n.*1578G>C
|
|
ENST00000647346.1:n.2729G>C
|
|
|
ENST00000299427.10:c.*17G>C
|
ENSP00000299427.6:n.*17G>C
|
|
ENST00000533371.5:c.*17G>C
|
ENSP00000437066.1:n.*17G>C
|
|
ENST00000611494.4:c.*37G>C
|
ENSP00000484546.1:n.*37G>C
|
|
NM_000391.3:c.*17G>C
|
NP_000382.3:n.*17G>C
|
|
NM_000391.4:c.*17G>C
MANE Select
|
NP_000382.3:n.*17G>C
|
|