ENST00000396705.10:c.516T>G
MANE Select
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ENSP00000379933.4:p.Gly172=
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ENST00000229270.8:c.627T>G
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ENSP00000229270.4:p.Gly209=
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ENST00000396705.9:c.516T>G
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ENSP00000379933.4:p.Gly172=
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ENST00000482209.1:n.199T>G
|
|
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ENST00000488464.6:c.270T>G
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ENSP00000475620.1:p.Gly90=
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ENST00000493987.5:c.270T>G
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ENSP00000475364.1:p.Gly90=
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ENST00000495834.1:c.270T>G
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ENSP00000475829.1:p.Gly90=
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ENST00000535434.5:c.270T>G
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ENSP00000443599.1:p.Gly90=
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ENST00000613953.4:c.627T>G
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ENSP00000484435.1:p.Gly209=
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NM_000365.5:c.516T>G
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NP_000356.1:p.Gly172=
|
|
NM_001159287.1:c.627T>G
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NP_001152759.1:p.Gly209=
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NM_001258026.1:c.270T>G
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NP_001244955.1:p.Gly90=
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XR_002957378.1:n.1249T>G
|
|
|
NM_000365.6:c.516T>G
MANE Select
|
NP_000356.1:p.Gly172=
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NM_001258026.2:c.270T>G
|
NP_001244955.1:p.Gly90=
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