ENST00000395762.7:c.1100C>G
MANE Select
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ENSP00000379111.2:p.Ala367Gly
|
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ENST00000170630.6:c.1055C>G
|
ENSP00000170630.3:p.Ala352Gly
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ENST00000395762.6:c.1100C>G
|
ENSP00000379111.2:p.Ala367Gly
|
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ENST00000543915.6:c.1100C>G
|
ENSP00000441667.2:p.Ala367Gly
|
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ENST00000565352.1:c.230-1651C>G
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ENSP00000461268.1:n.230-1651C>G
|
|
ENST00000565915.5:n.510C>G
|
|
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ENST00000568746.5:c.*1143C>G
|
ENSP00000455714.1:n.*1143C>G
|
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NM_000418.3:c.1100C>G
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NP_000409.1:p.Ala367Gly
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NM_001257406.1:c.1100C>G
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NP_001244335.1:p.Ala367Gly
|
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NM_001257407.1:c.1055C>G
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NP_001244336.1:p.Ala352Gly
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|
NM_001257997.1:c.620C>G
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NP_001244926.1:p.Ala207Gly
|
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XM_005255308.2:c.209C>G
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XP_005255365.1:p.Ala70Gly
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XM_006721043.1:c.149C>G
|
XP_006721106.1:p.Ala50Gly
|
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XM_011545825.1:c.1100C>G
|
XP_011544127.1:p.Ala367Gly
|
|
XM_011545826.1:c.1100C>G
|
XP_011544128.1:p.Ala367Gly
|
|
XM_011545827.1:c.1100C>G
|
XP_011544129.1:p.Ala367Gly
|
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XM_011545828.1:c.833C>G
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XP_011544130.1:p.Ala278Gly
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|
XM_011545829.1:c.803C>G
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XP_011544131.1:p.Ala268Gly
|
|
XM_011545830.1:c.803C>G
|
XP_011544132.1:p.Ala268Gly
|
|
XM_011545831.1:c.803C>G
|
XP_011544133.1:p.Ala268Gly
|
|
XM_011545832.1:c.803C>G
|
XP_011544134.1:p.Ala268Gly
|
|
XM_011545833.1:c.803C>G
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XP_011544135.1:p.Ala268Gly
|
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XM_011545834.1:c.677C>G
|
XP_011544136.1:p.Ala226Gly
|
|
XM_011545826.2:c.1100C>G
|
XP_011544128.1:p.Ala367Gly
|
|
XM_011545827.2:c.1100C>G
|
XP_011544129.1:p.Ala367Gly
|
|
XM_011545828.2:c.833C>G
|
XP_011544130.1:p.Ala278Gly
|
|
XM_011545830.2:c.803C>G
|
XP_011544132.1:p.Ala268Gly
|
|
XM_011545833.2:c.803C>G
|
XP_011544135.1:p.Ala268Gly
|
|
XM_011545834.2:c.677C>G
|
XP_011544136.1:p.Ala226Gly
|
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XM_017023211.1:c.*135C>G
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XP_016878700.1:n.*135C>G
|
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NM_000418.4:c.1100C>G
MANE Select
|
NP_000409.1:p.Ala367Gly
|
|
NM_001257406.2:c.1100C>G
|
NP_001244335.1:p.Ala367Gly
|
|
NM_001257407.2:c.1055C>G
|
NP_001244336.1:p.Ala352Gly
|
|
NM_001257997.2:c.620C>G
|
NP_001244926.1:p.Ala207Gly
|
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