ENST00000649368.1:c.1308C>G
MANE Select
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ENSP00000496793.1:p.Gly436=
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ENST00000343916.7:c.1308C>G
|
ENSP00000341640.3:p.Gly436=
|
|
ENST00000466192.5:n.1035C>G
|
|
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ENST00000469852.5:n.604C>G
|
|
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ENST00000481800.1:n.281C>G
|
|
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ENST00000490398.5:n.105C>G
|
|
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NM_001853.3:c.1308C>G
|
NP_001844.3:p.Gly436=
|
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XM_011528543.1:c.1308C>G
|
XP_011526845.1:p.Gly436=
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|
XM_011528544.1:c.1101C>G
|
XP_011526846.1:p.Gly367=
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XM_011528545.1:c.1308C>G
|
XP_011526847.1:p.Gly436=
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|
XM_011528546.1:c.1308C>G
|
XP_011526848.1:p.Gly436=
|
|
XM_011528547.1:c.1308C>G
|
XP_011526849.1:p.Gly436=
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|
XR_936499.1:n.1309C>G
|
|
|
NM_001853.4:c.1308C>G
MANE Select
|
NP_001844.3:p.Gly436=
|
|
XM_017027666.1:c.1308C>G
|
XP_016883155.1:p.Gly436=
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