ENST00000352511.5:c.1277A>G
MANE Select
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ENSP00000340361.3:p.Glu426Gly
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ENST00000352511.4:c.1277A>G
|
ENSP00000340361.3:p.Glu426Gly
|
|
ENST00000461232.1:n.5066A>G
|
|
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ENST00000465020.5:n.1363A>G
|
|
|
NM_001106.3:c.1277A>G
|
NP_001097.2:p.Glu426Gly
|
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XM_005265583.2:c.1340A>G
|
XP_005265640.1:p.Glu447Gly
|
|
XM_005265583.3:c.1340A>G
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XP_005265640.1:p.Glu447Gly
|
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XM_017007514.1:c.1319A>G
|
XP_016863003.1:p.Glu440Gly
|
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XM_017007515.2:c.1295A>G
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XP_016863004.1:p.Glu432Gly
|
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XM_017007516.1:c.1274A>G
|
XP_016863005.1:p.Glu425Gly
|
|
NM_001106.4:c.1277A>G
MANE Select
|
NP_001097.2:p.Glu426Gly
|
|