ENST00000681320.1:c.7776A>G
MANE Select
|
ENSP00000506558.1:p.Ala2592=
|
|
ENST00000328333.12:c.7776A>G
|
ENSP00000332371.8:p.Ala2592=
|
|
ENST00000459756.5:n.599A>G
|
|
|
ENST00000467985.1:n.622A>G
|
|
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ENST00000487017.5:n.4415A>G
|
|
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NM_000094.3:c.7776A>G , LRG_286t1:c.7776A>G
|
NP_000085.1:p.Ala2592=
|
|
XM_011533336.1:c.7803A>G
|
XP_011531638.1:p.Ala2601=
|
|
XM_011533337.1:c.7776A>G
|
XP_011531639.1:p.Ala2592=
|
|
XM_011533338.1:c.7743A>G
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XP_011531640.1:p.Ala2581=
|
|
XM_011533339.1:c.7803A>G
|
XP_011531641.1:p.Ala2601=
|
|
XR_940369.1:n.7839A>G
|
|
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XR_940370.1:n.7839A>G
|
|
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XR_940371.1:n.7839A>G
|
|
|
XR_940372.1:n.7813A>G
|
|
|
XM_017005688.1:c.7716A>G
|
XP_016861177.1:p.Ala2572=
|
|
XM_017005689.1:c.7776A>G
|
XP_016861178.1:p.Ala2592=
|
|
XR_001740003.1:n.7812A>G
|
|
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XR_001740004.1:n.7812A>G
|
|
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XR_001740005.1:n.7812A>G
|
|
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XR_001740006.1:n.7786A>G
|
|
|
NM_000094.4:c.7776A>G
MANE Select
|
NP_000085.1:p.Ala2592=
|
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