ENST00000395762.7:c.1403A>C
MANE Select
|
ENSP00000379111.2:p.Glu468Ala
|
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ENST00000170630.6:c.1358A>C
|
ENSP00000170630.3:p.Glu453Ala
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ENST00000395762.6:c.1403A>C
|
ENSP00000379111.2:p.Glu468Ala
|
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ENST00000543915.6:c.1403A>C
|
ENSP00000441667.2:p.Glu468Ala
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ENST00000565352.1:c.230-1348A>C
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ENSP00000461268.1:n.230-1348A>C
|
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ENST00000568746.5:c.*1446A>C
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ENSP00000455714.1:n.*1446A>C
|
|
NM_000418.3:c.1403A>C
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NP_000409.1:p.Glu468Ala
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NM_001257406.1:c.1403A>C
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NP_001244335.1:p.Glu468Ala
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|
NM_001257407.1:c.1358A>C
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NP_001244336.1:p.Glu453Ala
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NM_001257997.1:c.923A>C
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NP_001244926.1:p.Glu308Ala
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XM_005255308.2:c.512A>C
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XP_005255365.1:p.Glu171Ala
|
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XM_006721043.1:c.452A>C
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XP_006721106.1:p.Glu151Ala
|
|
XM_011545825.1:c.1403A>C
|
XP_011544127.1:p.Glu468Ala
|
|
XM_011545826.1:c.1403A>C
|
XP_011544128.1:p.Glu468Ala
|
|
XM_011545827.1:c.1403A>C
|
XP_011544129.1:p.Glu468Ala
|
|
XM_011545828.1:c.1136A>C
|
XP_011544130.1:p.Glu379Ala
|
|
XM_011545829.1:c.1106A>C
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XP_011544131.1:p.Glu369Ala
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|
XM_011545830.1:c.1106A>C
|
XP_011544132.1:p.Glu369Ala
|
|
XM_011545831.1:c.1106A>C
|
XP_011544133.1:p.Glu369Ala
|
|
XM_011545832.1:c.1106A>C
|
XP_011544134.1:p.Glu369Ala
|
|
XM_011545833.1:c.1106A>C
|
XP_011544135.1:p.Glu369Ala
|
|
XM_011545834.1:c.980A>C
|
XP_011544136.1:p.Glu327Ala
|
|
XM_011545826.2:c.1403A>C
|
XP_011544128.1:p.Glu468Ala
|
|
XM_011545827.2:c.1403A>C
|
XP_011544129.1:p.Glu468Ala
|
|
XM_011545828.2:c.1136A>C
|
XP_011544130.1:p.Glu379Ala
|
|
XM_011545830.2:c.1106A>C
|
XP_011544132.1:p.Glu369Ala
|
|
XM_011545833.2:c.1106A>C
|
XP_011544135.1:p.Glu369Ala
|
|
XM_011545834.2:c.980A>C
|
XP_011544136.1:p.Glu327Ala
|
|
XM_017023211.1:c.*438A>C
|
XP_016878700.1:n.*438A>C
|
|
NM_000418.4:c.1403A>C
MANE Select
|
NP_000409.1:p.Glu468Ala
|
|
NM_001257406.2:c.1403A>C
|
NP_001244335.1:p.Glu468Ala
|
|
NM_001257407.2:c.1358A>C
|
NP_001244336.1:p.Glu453Ala
|
|
NM_001257997.2:c.923A>C
|
NP_001244926.1:p.Glu308Ala
|
|