ENST00000249806.11:c.776G>A
MANE Select
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ENSP00000249806.5:p.Gly259Asp
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ENST00000562767.2:c.84-10672G>A
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ENSP00000456336.1:n.84-10672G>A
|
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ENST00000565471.6:c.317G>A
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ENSP00000457384.1:p.Gly106Asp
|
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ENST00000635747.1:c.*679G>A
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ENSP00000490627.1:n.*679G>A
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ENST00000636212.1:c.*446G>A
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ENSP00000489851.1:n.*446G>A
|
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ENST00000636674.1:n.1878G>A
|
|
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ENST00000636964.1:n.2304G>A
|
|
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ENST00000637054.1:c.198+10236G>A
|
ENSP00000490807.1:n.198+10236G>A
|
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ENST00000637329.1:c.745G>A
|
|
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ENST00000637450.1:c.*430G>A
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ENSP00000490204.1:n.*430G>A
|
|
ENST00000637494.1:c.488G>A
|
ENSP00000490057.1:p.Gly163Asp
|
|
ENST00000637667.1:c.677G>A
|
ENSP00000489843.1:p.Gly226Asp
|
|
ENST00000637823.1:c.601G>A
|
|
|
ENST00000637888.1:c.198+10236G>A
|
ENSP00000490546.1:n.198+10236G>A
|
|
ENST00000638076.1:c.*379G>A
|
ENSP00000490373.1:n.*379G>A
|
|
ENST00000638144.1:n.419G>A
|
|
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ENST00000646164.1:c.39-8619G>A
|
|
|
ENST00000249806.9:c.776G>A
|
ENSP00000249806.5:p.Gly259Asp
|
|
ENST00000538696.5:c.872G>A
|
ENSP00000445770.1:p.Gly291Asp
|
|
ENST00000562767.1:c.84-10672G>A
|
ENSP00000456336.1:n.84-10672G>A
|
|
ENST00000565471.5:c.317G>A
|
ENSP00000457384.1:p.Gly106Asp
|
|
ENST00000566347.5:c.587G>A
|
ENSP00000457783.1:p.Gly196Asp
|
|
ENST00000567060.5:c.*174G>A
|
ENSP00000454818.1:n.*174G>A
|
|
NM_017882.2:c.776G>A
|
NP_060352.1:p.Gly259Asp
|
|
NM_017882.3:c.776G>A
MANE Select
|
NP_060352.1:p.Gly259Asp
|
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