ENST00000218099.7:c.1046G=
MANE Select
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ENSP00000218099.2:p.Gly349=
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ENST00000643157.1:n.1713G=
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|
|
ENST00000218099.6:c.1046G=
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ENSP00000218099.2:p.Gly349=
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ENST00000394090.2:c.932G=
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ENSP00000377650.2:p.Gly311=
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NM_000133.3:c.1046G= , LRG_556t1:c.1046G=
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NP_000124.1:p.Gly349=
|
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NM_001313913.1:c.932G=
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NP_001300842.1:p.Gly311=
|
|
XM_005262397.3:c.917G=
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XP_005262454.1:p.Gly306=
|
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XM_005262397.4:c.917G=
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XP_005262454.1:p.Gly306=
|
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NM_000133.4:c.1046G=
MANE Select
|
NP_000124.1:p.Gly349=
|
|
NM_001313913.2:c.932G=
|
NP_001300842.1:p.Gly311=
|
|