ENST00000217958.8:c.677G>T
MANE Select
|
ENSP00000217958.3:p.Gly226Val
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|
ENST00000217958.7:c.677G>T
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ENSP00000217958.3:p.Gly226Val
|
|
ENST00000340200.5:c.578G>T
|
ENSP00000345963.5:p.Gly193Val
|
|
ENST00000361815.9:c.*142G>T
|
ENSP00000354906.5:n.*142G>T
|
|
ENST00000372295.5:c.554G>T
|
ENSP00000361369.1:p.Gly185Val
|
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ENST00000372296.5:c.*142G>T
|
ENSP00000361370.1:n.*142G>T
|
|
NM_002814.3:c.677G>T
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NP_002805.1:p.Gly226Val
|
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NM_170750.2:c.*142G>T
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NP_736606.1:n.*142G>T
|
|
NM_002814.4:c.677G>T
MANE Select
|
NP_002805.1:p.Gly226Val
|
|
NM_170750.3:c.*142G>T
|
NP_736606.1:n.*142G>T
|
|