ENST00000322213.9:c.1468G>T
MANE Select
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ENSP00000323421.3:p.Asp490Tyr
|
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ENST00000674590.1:c.700G>T
|
ENSP00000502626.1:p.Asp234Tyr
|
|
ENST00000675065.1:n.820G>T
|
|
|
ENST00000675504.1:c.1402G>T
|
ENSP00000502524.1:p.Asp468Tyr
|
|
ENST00000322213.8:c.1468G>T
|
ENSP00000323421.3:p.Asp490Tyr
|
|
ENST00000375340.10:c.1402G>T
|
ENSP00000364489.7:p.Asp468Tyr
|
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NM_001281463.1:c.1402G>T , LRG_773t1:c.1402G>T
|
NP_001268392.1:p.Asp468Tyr
|
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NM_006306.3:c.1468G>T , LRG_773t2:c.1468G>T
|
NP_006297.2:p.Asp490Tyr
|
|
NM_006306.4:c.1468G>T
MANE Select
|
NP_006297.2:p.Asp490Tyr
|
|