ENST00000456935.7:c.1451G>A
MANE Select
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ENSP00000395473.2:p.Arg484Lys
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ENST00000221363.8:c.1448G>A
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ENSP00000221363.4:p.Arg483Lys
|
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ENST00000433513.5:n.57G>A
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|
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ENST00000456935.6:c.1451G>A
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ENSP00000395473.2:p.Arg484Lys
|
|
ENST00000466794.5:n.1350G>A
|
|
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ENST00000495617.1:n.627G>A
|
|
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ENST00000593686.1:c.61G>A
|
|
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ENST00000595880.5:n.48G>A
|
|
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NM_000528.3:c.1451G>A
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NP_000519.2:p.Arg484Lys
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NM_001173498.1:c.1448G>A
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NP_001166969.1:p.Arg483Lys
|
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XM_005259913.1:c.1454G>A
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XP_005259970.1:p.Arg485Lys
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XM_011528017.1:c.350G>A
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XP_011526319.1:p.Arg117Lys
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|
XM_005259913.2:c.1454G>A
|
XP_005259970.1:p.Arg485Lys
|
|
XM_024451518.1:c.350G>A
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XP_024307286.1:p.Arg117Lys
|
|
NM_000528.4:c.1451G>A
MANE Select
|
NP_000519.2:p.Arg484Lys
|
|
NM_001173498.2:c.1448G>A
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NP_001166969.1:p.Arg483Lys
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