ENST00000347147.9:c.1045G>A
MANE Select
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ENSP00000333355.6:p.Gly349Ser
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ENST00000347147.8:c.1045G>A
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ENSP00000333355.6:p.Gly349Ser
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ENST00000381975.7:c.1041G>A
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ENSP00000371402.3:p.Gln347=
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ENST00000392432.6:c.1186G>A
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ENSP00000376227.2:p.Gly396Ser
|
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ENST00000419280.5:c.*341G>A
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ENSP00000414077.1:n.*341G>A
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ENST00000429560.1:c.237G>A
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ENSP00000403053.1:p.Gln79=
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ENST00000432352.5:c.319G>A
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ENSP00000409963.1:p.Gly107Ser
|
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ENST00000452358.5:c.544G>A
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ENSP00000414333.1:p.Gly182Ser
|
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ENST00000467284.1:n.91G>A
|
|
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ENST00000473092.5:c.1045G>A
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ENSP00000418674.1:p.Gly349Ser
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ENST00000477651.5:n.809G>A
|
|
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NM_001011655.2:c.1045G>A
|
NP_001011655.1:p.Gly349Ser
|
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NM_001166305.1:c.1186G>A
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NP_001159777.1:p.Gly396Ser
|
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NM_001166306.1:c.1041G>A
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NP_001159778.1:p.Gln347=
|
|
NM_138399.4:c.1045G>A
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NP_612408.3:p.Gly349Ser
|
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XM_005269371.3:c.1045G>A
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XP_005269428.1:p.Gly349Ser
|
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XM_011513318.1:c.1195G>A
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XP_011511620.1:p.Gly399Ser
|
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XM_011513319.1:c.1132G>A
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XP_011511621.1:p.Gly378Ser
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XM_011513320.1:c.1243G>A
|
XP_011511622.1:p.Gly415Ser
|
|
XM_011513321.1:c.1111G>A
|
XP_011511623.1:p.Gly371Ser
|
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XM_011513322.1:c.1102G>A
|
XP_011511624.1:p.Gly368Ser
|
|
XM_011513323.1:c.940G>A
|
XP_011511625.1:p.Gly314Ser
|
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XM_005269371.4:c.1045G>A
|
XP_005269428.1:p.Gly349Ser
|
|
XM_011513318.2:c.1195G>A
|
XP_011511620.1:p.Gly399Ser
|
|
XM_011513319.2:c.1132G>A
|
XP_011511621.1:p.Gly378Ser
|
|
XM_011513320.2:c.1243G>A
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XP_011511622.1:p.Gly415Ser
|
|
XM_011513321.2:c.1111G>A
|
XP_011511623.1:p.Gly371Ser
|
|
XM_011513322.2:c.1102G>A
|
XP_011511624.1:p.Gly368Ser
|
|
XM_017007517.1:c.1054G>A
|
XP_016863006.1:p.Gly352Ser
|
|
XM_017007518.1:c.1054G>A
|
XP_016863007.1:p.Gly352Ser
|
|
NM_001011655.3:c.1045G>A
MANE Select
|
NP_001011655.1:p.Gly349Ser
|
|
NM_001166305.2:c.1186G>A
|
NP_001159777.1:p.Gly396Ser
|
|
NM_001166306.2:c.1041G>A
|
NP_001159778.1:p.Gln347=
|
|
NM_138399.5:c.1045G>A
|
NP_612408.3:p.Gly349Ser
|
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