ENST00000381750.9:c.584+129A>G
MANE Select
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ENSP00000371169.4:n.584+129A>G
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|
ENST00000381750.8:c.584+129A>G
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ENSP00000371169.4:n.584+129A>G
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|
ENST00000442869.5:c.110+129A>G
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ENSP00000412000.2:n.110+129A>G
|
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ENST00000473230.1:n.288+1166A>G
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|
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NM_001286699.1:c.110+129A>G
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NP_001273628.1:n.110+129A>G
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NM_001286700.1:c.110+129A>G
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NP_001273629.1:n.110+129A>G
|
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NM_005772.4:c.584+129A>G
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NP_005763.3:n.584+129A>G
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XM_006716715.2:c.260+129A>G
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XP_006716778.1:n.260+129A>G
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XM_006716715.3:c.260+129A>G
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XP_006716778.1:n.260+129A>G
|
|
NM_005772.5:c.584+129A>G
MANE Select
|
NP_005763.3:n.584+129A>G
|
|
NM_001286699.2:c.110+129A>G
|
NP_001273628.1:n.110+129A>G
|
|
NM_001286700.2:c.110+129A>G
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NP_001273629.1:n.110+129A>G
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