ENST00000375448.4:c.1063G=
MANE Select
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ENSP00000364597.4:p.Gly355=
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|
ENST00000468945.1:n.122G=
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|
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ENST00000487048.5:n.30G=
|
|
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NM_012387.2:c.1063G=
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NP_036519.2:p.Gly355=
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|
XM_011541150.1:c.877G=
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XP_011539452.1:p.Gly293=
|
|
XM_011541151.1:c.1063G=
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XP_011539453.1:p.Gly355=
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|
XM_011541152.1:c.526G=
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XP_011539454.1:p.Gly176=
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|
XM_011541153.1:c.1063G=
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XP_011539455.1:p.Gly355=
|
|
XM_011541154.1:c.1063G=
|
XP_011539456.1:p.Gly355=
|
|
XM_011541155.1:c.1063G=
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XP_011539457.1:p.Gly355=
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|
XM_011541156.1:c.1063G=
|
XP_011539458.1:p.Gly355=
|
|
XM_011541157.1:c.172G=
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XP_011539459.1:p.Gly58=
|
|
XM_011541154.2:c.1063G=
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XP_011539456.1:p.Gly355=
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|
NM_012387.3:c.1063G=
MANE Select
|
NP_036519.2:p.Gly355=
|
|