ENST00000378585.7:c.87C>G
MANE Select
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ENSP00000367848.4:p.Gly29=
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ENST00000638411.1:c.87C>G
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ENSP00000491632.1:p.Gly29=
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ENST00000638604.1:n.151C>G
|
|
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ENST00000638771.1:c.87C>G
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ENSP00000492435.1:p.Gly29=
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ENST00000639045.1:c.*73C>G
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ENSP00000491997.1:n.*73C>G
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ENST00000639777.1:n.691C>G
|
|
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ENST00000639935.1:n.124C>G
|
|
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ENST00000640030.1:c.27C>G
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ENSP00000491411.1:p.Gly9=
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ENST00000640067.1:c.87C>G
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ENSP00000491844.1:p.Gly29=
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ENST00000640423.1:n.96C>G
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|
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ENST00000640949.1:c.87C>G
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ENSP00000492500.1:p.Gly29=
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|
ENST00000378585.5:c.87C>G
|
ENSP00000367848.4:p.Gly29=
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NM_000815.4:c.87C>G
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NP_000806.2:p.Gly29=
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XM_011541194.1:c.126C>G
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XP_011539496.1:p.Gly42=
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XM_011541194.3:c.126C>G
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XP_011539496.1:p.Gly42=
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XM_017000936.1:c.792C>G
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XP_016856425.1:p.Gly264=
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NM_000815.5:c.87C>G
MANE Select
|
NP_000806.2:p.Gly29=
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