ENST00000324662.8:c.1377G>A
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ENSP00000313419.4:p.Glu459=
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ENST00000538922.8:c.1377G>A
MANE Select
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ENSP00000437940.2:p.Glu459=
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ENST00000324662.7:c.1377G>A
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ENSP00000313419.3:p.Glu459=
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ENST00000538922.5:c.1377G>A
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ENSP00000437940.1:p.Glu459=
|
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ENST00000565089.5:n.1811G>A
|
|
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ENST00000567368.1:n.517G>A
|
|
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ENST00000567541.5:c.1377G>A
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ENSP00000456201.1:p.Glu459=
|
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ENST00000611258.4:c.1376G>A
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ENSP00000481090.1:p.Ser459Asn
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NM_001178098.1:c.1377G>A
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NP_001171569.1:p.Glu459=
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NM_001770.5:c.1377G>A , LRG_35t1:c.1377G>A
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NP_001761.3:p.Glu459=
|
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XM_006721103.2:c.1110G>A
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XP_006721166.1:p.Glu370=
|
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XM_006721103.3:c.1110G>A
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XP_006721166.1:p.Glu370=
|
|
XM_017023893.1:c.1110G>A
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XP_016879382.1:p.Glu370=
|
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NM_001178098.2:c.1377G>A
|
NP_001171569.1:p.Glu459=
|
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NM_001770.6:c.1377G>A
MANE Select
|
NP_001761.3:p.Glu459=
|
|
NM_001385732.1:c.1110G>A
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NP_001372661.1:p.Glu370=
|
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NR_169755.1:n.1719G>A
|
|
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