ENST00000347147.9:c.1112T>G
MANE Select
|
ENSP00000333355.6:p.Val371Gly
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ENST00000347147.8:c.1112T>G
|
ENSP00000333355.6:p.Val371Gly
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|
ENST00000381975.7:c.1108T>G
|
ENSP00000371402.3:p.Ser370Ala
|
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ENST00000392432.6:c.1253T>G
|
ENSP00000376227.2:p.Val418Gly
|
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ENST00000419280.5:c.*408T>G
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ENSP00000414077.1:n.*408T>G
|
|
ENST00000429560.1:c.304T>G
|
ENSP00000403053.1:p.Ser102Ala
|
|
ENST00000432352.5:c.386T>G
|
ENSP00000409963.1:p.Val129Gly
|
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ENST00000452358.5:c.611T>G
|
ENSP00000414333.1:p.Val204Gly
|
|
ENST00000467284.1:n.158T>G
|
|
|
ENST00000473092.5:c.1112T>G
|
ENSP00000418674.1:p.Val371Gly
|
|
ENST00000477651.5:n.876T>G
|
|
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NM_001011655.2:c.1112T>G
|
NP_001011655.1:p.Val371Gly
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|
NM_001166305.1:c.1253T>G
|
NP_001159777.1:p.Val418Gly
|
|
NM_001166306.1:c.1108T>G
|
NP_001159778.1:p.Ser370Ala
|
|
NM_138399.4:c.1112T>G
|
NP_612408.3:p.Val371Gly
|
|
XM_005269371.3:c.1112T>G
|
XP_005269428.1:p.Val371Gly
|
|
XM_011513318.1:c.1262T>G
|
XP_011511620.1:p.Val421Gly
|
|
XM_011513319.1:c.1199T>G
|
XP_011511621.1:p.Val400Gly
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|
XM_011513320.1:c.1310T>G
|
XP_011511622.1:p.Val437Gly
|
|
XM_011513321.1:c.1178T>G
|
XP_011511623.1:p.Val393Gly
|
|
XM_011513322.1:c.1169T>G
|
XP_011511624.1:p.Val390Gly
|
|
XM_011513323.1:c.1007T>G
|
XP_011511625.1:p.Val336Gly
|
|
XM_005269371.4:c.1112T>G
|
XP_005269428.1:p.Val371Gly
|
|
XM_011513318.2:c.1262T>G
|
XP_011511620.1:p.Val421Gly
|
|
XM_011513319.2:c.1199T>G
|
XP_011511621.1:p.Val400Gly
|
|
XM_011513320.2:c.1310T>G
|
XP_011511622.1:p.Val437Gly
|
|
XM_011513321.2:c.1178T>G
|
XP_011511623.1:p.Val393Gly
|
|
XM_011513322.2:c.1169T>G
|
XP_011511624.1:p.Val390Gly
|
|
XM_017007517.1:c.1121T>G
|
XP_016863006.1:p.Val374Gly
|
|
XM_017007518.1:c.1121T>G
|
XP_016863007.1:p.Val374Gly
|
|
NM_001011655.3:c.1112T>G
MANE Select
|
NP_001011655.1:p.Val371Gly
|
|
NM_001166305.2:c.1253T>G
|
NP_001159777.1:p.Val418Gly
|
|
NM_001166306.2:c.1108T>G
|
NP_001159778.1:p.Ser370Ala
|
|
NM_138399.5:c.1112T>G
|
NP_612408.3:p.Val371Gly
|
|