ENST00000347147.9:c.1108C>G
MANE Select
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ENSP00000333355.6:p.Gln370Glu
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ENST00000347147.8:c.1108C>G
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ENSP00000333355.6:p.Gln370Glu
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|
ENST00000381975.7:c.1104C>G
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ENSP00000371402.3:p.Phe368Leu
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ENST00000392432.6:c.1249C>G
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ENSP00000376227.2:p.Gln417Glu
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ENST00000419280.5:c.*404C>G
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ENSP00000414077.1:n.*404C>G
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|
ENST00000429560.1:c.300C>G
|
ENSP00000403053.1:p.Phe100Leu
|
|
ENST00000432352.5:c.382C>G
|
ENSP00000409963.1:p.Gln128Glu
|
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ENST00000452358.5:c.607C>G
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ENSP00000414333.1:p.Gln203Glu
|
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ENST00000467284.1:n.154C>G
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|
|
ENST00000473092.5:c.1108C>G
|
ENSP00000418674.1:p.Gln370Glu
|
|
ENST00000477651.5:n.872C>G
|
|
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NM_001011655.2:c.1108C>G
|
NP_001011655.1:p.Gln370Glu
|
|
NM_001166305.1:c.1249C>G
|
NP_001159777.1:p.Gln417Glu
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|
NM_001166306.1:c.1104C>G
|
NP_001159778.1:p.Phe368Leu
|
|
NM_138399.4:c.1108C>G
|
NP_612408.3:p.Gln370Glu
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|
XM_005269371.3:c.1108C>G
|
XP_005269428.1:p.Gln370Glu
|
|
XM_011513318.1:c.1258C>G
|
XP_011511620.1:p.Gln420Glu
|
|
XM_011513319.1:c.1195C>G
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XP_011511621.1:p.Gln399Glu
|
|
XM_011513320.1:c.1306C>G
|
XP_011511622.1:p.Gln436Glu
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|
XM_011513321.1:c.1174C>G
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XP_011511623.1:p.Gln392Glu
|
|
XM_011513322.1:c.1165C>G
|
XP_011511624.1:p.Gln389Glu
|
|
XM_011513323.1:c.1003C>G
|
XP_011511625.1:p.Gln335Glu
|
|
XM_005269371.4:c.1108C>G
|
XP_005269428.1:p.Gln370Glu
|
|
XM_011513318.2:c.1258C>G
|
XP_011511620.1:p.Gln420Glu
|
|
XM_011513319.2:c.1195C>G
|
XP_011511621.1:p.Gln399Glu
|
|
XM_011513320.2:c.1306C>G
|
XP_011511622.1:p.Gln436Glu
|
|
XM_011513321.2:c.1174C>G
|
XP_011511623.1:p.Gln392Glu
|
|
XM_011513322.2:c.1165C>G
|
XP_011511624.1:p.Gln389Glu
|
|
XM_017007517.1:c.1117C>G
|
XP_016863006.1:p.Gln373Glu
|
|
XM_017007518.1:c.1117C>G
|
XP_016863007.1:p.Gln373Glu
|
|
NM_001011655.3:c.1108C>G
MANE Select
|
NP_001011655.1:p.Gln370Glu
|
|
NM_001166305.2:c.1249C>G
|
NP_001159777.1:p.Gln417Glu
|
|
NM_001166306.2:c.1104C>G
|
NP_001159778.1:p.Phe368Leu
|
|
NM_138399.5:c.1108C>G
|
NP_612408.3:p.Gln370Glu
|
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