ENST00000356392.9:c.1297G>T
MANE Select
|
ENSP00000348757.3:p.Glu433Ter
|
|
ENST00000356392.8:c.1297G>T
|
ENSP00000348757.3:p.Glu433Ter
|
|
ENST00000586836.5:c.724G>T
|
ENSP00000467429.1:p.Glu242Ter
|
|
ENST00000591179.5:c.1117G>T
|
ENSP00000466800.1:p.Glu373Ter
|
|
ENST00000591345.5:c.*1216G>T
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ENSP00000467313.1:n.*1216G>T
|
|
NM_001302453.1:c.1135G>T
|
NP_001289382.1:p.Glu379Ter
|
|
NM_001302454.1:c.1117G>T
|
NP_001289383.1:p.Glu373Ter
|
|
NM_145045.4:c.1297G>T
|
NP_659482.3:p.Glu433Ter
|
|
NM_145045.5:c.1297G>T
MANE Select
|
NP_659482.3:p.Glu433Ter
|
|
NM_001302454.2:c.1117G>T
|
NP_001289383.1:p.Glu373Ter
|
|