ENST00000366577.10:c.2672T>G
MANE Select
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ENSP00000355536.5:p.Val891Gly
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ENST00000535889.6:c.2519T>G
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ENSP00000441845.1:p.Val840Gly
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ENST00000650888.1:c.*1714T>G
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ENSP00000498393.1:n.*1714T>G
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ENST00000651455.1:c.*1416T>G
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ENSP00000498963.1:n.*1416T>G
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ENST00000674797.2:c.2324T>G
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ENSP00000502299.2:p.Val775Gly
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ENST00000679569.1:n.2986T>G
|
|
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ENST00000679842.1:c.2483T>G
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ENSP00000506109.1:p.Val828Gly
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ENST00000680454.1:n.3116T>G
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ENST00000681102.1:c.2492T>G
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ENSP00000505600.1:p.Val831Gly
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ENST00000681177.1:c.2234T>G
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ENSP00000506327.1:p.Val745Gly
|
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ENST00000681937.1:n.2866T>G
|
|
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ENST00000366576.3:c.1334T>G
|
ENSP00000355535.3:p.Val445Gly
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ENST00000366577.9:c.2672T>G
|
ENSP00000355536.5:p.Val891Gly
|
|
ENST00000535889.5:c.2519T>G
|
ENSP00000441845.1:p.Val840Gly
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|
NM_000254.2:c.2672T>G
|
NP_000245.2:p.Val891Gly
|
|
NM_001291939.1:c.2519T>G
|
NP_001278868.1:p.Val840Gly
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NM_001291940.1:c.1451T>G
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NP_001278869.1:p.Val484Gly
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XM_005273141.3:c.2669T>G
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XP_005273198.1:p.Val890Gly
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XM_006711769.2:c.2672T>G
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XP_006711832.1:p.Val891Gly
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XM_006711770.1:c.1736T>G
|
XP_006711833.1:p.Val579Gly
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XM_011544193.1:c.2483T>G
|
XP_011542495.1:p.Val828Gly
|
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XM_011544194.1:c.2840T>G
|
XP_011542496.1:p.Val947Gly
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XM_005273141.5:c.2669T>G
|
XP_005273198.1:p.Val890Gly
|
|
XM_006711770.3:c.1736T>G
|
XP_006711833.1:p.Val579Gly
|
|
XM_011544194.3:c.2840T>G
|
XP_011542496.1:p.Val947Gly
|
|
XM_017001329.2:c.2687T>G
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XP_016856818.1:p.Val896Gly
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XM_017001330.2:c.2651T>G
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XP_016856819.1:p.Val884Gly
|
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NM_001291940.2:c.1451T>G
|
NP_001278869.1:p.Val484Gly
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|
NM_000254.3:c.2672T>G
MANE Select
|
NP_000245.2:p.Val891Gly
|
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