ENST00000456935.7:c.1391A>G
MANE Select
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ENSP00000395473.2:p.Gln464Arg
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ENST00000221363.8:c.1388A>G
|
ENSP00000221363.4:p.Gln463Arg
|
|
ENST00000456935.6:c.1391A>G
|
ENSP00000395473.2:p.Gln464Arg
|
|
ENST00000465830.1:n.555A>G
|
|
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ENST00000466794.5:n.1290A>G
|
|
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ENST00000495617.1:n.567A>G
|
|
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ENST00000593686.1:c.1A>G
|
|
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NM_000528.3:c.1391A>G
|
NP_000519.2:p.Gln464Arg
|
|
NM_001173498.1:c.1388A>G
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NP_001166969.1:p.Gln463Arg
|
|
XM_005259913.1:c.1394A>G
|
XP_005259970.1:p.Gln465Arg
|
|
XM_011528017.1:c.290A>G
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XP_011526319.1:p.Gln97Arg
|
|
XM_005259913.2:c.1394A>G
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XP_005259970.1:p.Gln465Arg
|
|
XM_024451518.1:c.290A>G
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XP_024307286.1:p.Gln97Arg
|
|
NM_000528.4:c.1391A>G
MANE Select
|
NP_000519.2:p.Gln464Arg
|
|
NM_001173498.2:c.1388A>G
|
NP_001166969.1:p.Gln463Arg
|
|