ENST00000688602.1:c.169A>G
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|
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ENST00000689936.1:c.151A>G
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ENST00000359596.8:c.11759A>G
MANE Select
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ENSP00000352608.2:p.Asp3920Gly
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ENST00000355481.8:c.11744A>G
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ENSP00000347667.3:p.Asp3915Gly
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ENST00000359596.7:c.11759A>G
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ENSP00000352608.2:p.Asp3920Gly
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ENST00000360985.7:c.11741A>G
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ENSP00000354254.4:p.Asp3914Gly
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ENST00000593322.1:c.368A>G
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|
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ENST00000594335.5:c.5128A>G
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NM_000540.2:c.11759A>G , LRG_766t1:c.11759A>G
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NP_000531.2:p.Asp3920Gly
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NM_001042723.1:c.11744A>G
|
NP_001036188.1:p.Asp3915Gly
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XM_006723317.1:c.11741A>G
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XP_006723380.1:p.Asp3914Gly
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XM_006723319.1:c.11726A>G
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XP_006723382.1:p.Asp3909Gly
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|
XM_011527204.1:c.11756A>G
|
XP_011525506.1:p.Asp3919Gly
|
|
XM_011527205.1:c.11759A>G
|
XP_011525507.1:p.Asp3920Gly
|
|
XM_006723317.2:c.11741A>G
|
XP_006723380.1:p.Asp3914Gly
|
|
XM_006723319.2:c.11726A>G
|
XP_006723382.1:p.Asp3909Gly
|
|
XM_011527205.2:c.11759A>G
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XP_011525507.1:p.Asp3920Gly
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NM_000540.3:c.11759A>G
MANE Select
|
NP_000531.2:p.Asp3920Gly
|
|
NM_001042723.2:c.11744A>G
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NP_001036188.1:p.Asp3915Gly
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