ENST00000378585.7:c.174C>G
MANE Select
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ENSP00000367848.4:p.Gly58=
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ENST00000638411.1:c.174C>G
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ENSP00000491632.1:p.Gly58=
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ENST00000638604.1:n.238C>G
|
|
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ENST00000638771.1:c.174C>G
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ENSP00000492435.1:p.Gly58=
|
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ENST00000639045.1:c.*160C>G
|
ENSP00000491997.1:n.*160C>G
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ENST00000639777.1:n.778C>G
|
|
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ENST00000639935.1:n.211C>G
|
|
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ENST00000640030.1:c.114C>G
|
ENSP00000491411.1:p.Gly38=
|
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ENST00000640067.1:c.174C>G
|
ENSP00000491844.1:p.Gly58=
|
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ENST00000640423.1:n.183C>G
|
|
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ENST00000640949.1:c.174C>G
|
ENSP00000492500.1:p.Gly58=
|
|
ENST00000378585.5:c.174C>G
|
ENSP00000367848.4:p.Gly58=
|
|
NM_000815.4:c.174C>G
|
NP_000806.2:p.Gly58=
|
|
XM_011541194.1:c.213C>G
|
XP_011539496.1:p.Gly71=
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|
XM_011541194.3:c.213C>G
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XP_011539496.1:p.Gly71=
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XM_017000936.1:c.879C>G
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XP_016856425.1:p.Gly293=
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NM_000815.5:c.174C>G
MANE Select
|
NP_000806.2:p.Gly58=
|
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