ENST00000251654.9:c.507A=
MANE Select
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ENSP00000251654.4:p.Gly169=
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ENST00000251654.8:c.507A=
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ENSP00000251654.4:p.Gly169=
|
|
ENST00000459873.1:c.258A=
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ENSP00000419293.1:p.Gly86=
|
|
ENST00000462542.5:c.374A=
|
|
|
ENST00000462637.5:c.438A=
|
ENSP00000420391.1:p.Gly146=
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|
ENST00000465176.5:n.469A=
|
|
|
ENST00000466072.5:c.507A=
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ENSP00000420158.1:p.Gly169=
|
|
ENST00000468777.5:c.600A=
|
ENSP00000419129.1:p.Gly200=
|
|
ENST00000469217.5:c.567A=
|
ENSP00000419027.1:p.Gly189=
|
|
ENST00000471595.5:c.507A=
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ENSP00000417549.1:p.Gly169=
|
|
ENST00000473073.1:n.464A=
|
|
|
ENST00000474833.5:n.168+11471A=
|
|
|
ENST00000475214.5:n.421A=
|
|
|
ENST00000478469.5:c.507A=
|
ENSP00000420759.1:p.Gly169=
|
|
ENST00000482086.5:c.159A=
|
ENSP00000417253.1:p.Gly53=
|
|
ENST00000483687.5:c.450A=
|
ENSP00000420639.1:p.Gly150=
|
|
ENST00000484181.5:c.507A=
|
ENSP00000417937.1:p.Gly169=
|
|
ENST00000490504.5:c.372+5406A=
|
ENSP00000418307.1:n.372+5406A=
|
|
NM_000532.4:c.507A=
|
NP_000523.2:p.Gly169=
|
|
NM_001178014.1:c.567A=
|
NP_001171485.1:p.Gly189=
|
|
XM_011512873.1:c.507A=
|
XP_011511175.1:p.Gly169=
|
|
XM_011512873.2:c.507A=
|
XP_011511175.1:p.Gly169=
|
|
NM_000532.5:c.507A=
MANE Select
|
NP_000523.2:p.Gly169=
|
|
NM_001178014.2:c.567A=
|
NP_001171485.1:p.Gly189=
|
|