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NM_000170.3:c.2901G>T
MANE Select
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NP_000161.2:p.Glu967Asp
|
|
ENST00000321612.8:c.2901G>T
MANE Select
|
ENSP00000370737.4:p.Glu967Asp
|
|
NM_000170.2:c.2901G>T , LRG_643t1:c.2901G>T
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NP_000161.2:p.Glu967Asp
|
|
ENST00000321612.6:c.2901G>T
|
ENSP00000370737.3:p.Glu967Asp
|
|
ENST00000477960.1:n.482G>T
|
|
|
ENST00000638233.1:n.1336G>T
|
|
|
ENST00000638274.1:c.53G>T
|
|
|
ENST00000638661.1:c.1101G>T
|
ENSP00000491369.1:p.Glu367Asp
|
|
ENST00000638694.1:n.1088G>T
|
|
|
ENST00000639318.1:c.1005G>T
|
ENSP00000491932.1:p.Glu335Asp
|
|
ENST00000639364.1:n.2601G>T
|
|
|
ENST00000639443.1:n.2469G>T
|
|
|
ENST00000639461.1:n.2002G>T
|
|
|
ENST00000639639.1:c.603G>T
|
ENSP00000491312.1:p.Glu201Asp
|
|
ENST00000639954.1:n.2609G>T
|
|
|
ENST00000640505.1:n.1140G>T
|
|