ENST00000378585.7:c.178G=
MANE Select
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ENSP00000367848.4:p.Gly60=
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ENST00000638411.1:c.178G=
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ENSP00000491632.1:p.Gly60=
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|
ENST00000638604.1:n.242G=
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|
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ENST00000638771.1:c.178G=
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ENSP00000492435.1:p.Gly60=
|
|
ENST00000639045.1:c.*164G=
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ENSP00000491997.1:n.*164G=
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ENST00000639777.1:n.782G=
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|
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ENST00000639935.1:n.215G=
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|
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ENST00000640030.1:c.118G=
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ENSP00000491411.1:p.Gly40=
|
|
ENST00000640067.1:c.178G=
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ENSP00000491844.1:p.Gly60=
|
|
ENST00000640423.1:n.187G=
|
|
|
ENST00000640949.1:c.178G=
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ENSP00000492500.1:p.Gly60=
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|
ENST00000378585.5:c.178G=
|
ENSP00000367848.4:p.Gly60=
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|
NM_000815.4:c.178G=
|
NP_000806.2:p.Gly60=
|
|
XM_011541194.1:c.217G=
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XP_011539496.1:p.Gly73=
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|
XM_011541194.3:c.217G=
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XP_011539496.1:p.Gly73=
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XM_017000936.1:c.883G=
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XP_016856425.1:p.Gly295=
|
|
NM_000815.5:c.178G=
MANE Select
|
NP_000806.2:p.Gly60=
|
|