ENST00000682424.1:c.962G>C
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ENSP00000507321.1:p.Gly321Ala
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ENST00000299427.12:c.1076G>C
MANE Select
|
ENSP00000299427.6:p.Gly359Ala
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ENST00000436873.7:c.313G>C
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ENST00000524924.2:n.196G>C
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ENST00000533371.6:c.347G>C
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ENSP00000437066.1:p.Gly116Ala
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ENST00000642892.1:c.347G>C
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ENSP00000494165.1:p.Gly116Ala
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ENST00000643342.1:c.166G>C
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|
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ENST00000643439.1:c.*816G>C
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ENSP00000495849.1:n.*816G>C
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ENST00000643479.1:n.1262G>C
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ENST00000643516.1:c.585G>C
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ENST00000644218.1:c.887G>C
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ENSP00000493574.1:p.Gly296Ala
|
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ENST00000644683.1:c.*529G>C
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ENSP00000494085.1:n.*529G>C
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ENST00000644810.1:c.797G>C
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ENSP00000495895.1:p.Gly266Ala
|
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ENST00000644831.1:n.1252G>C
|
|
|
ENST00000644933.1:c.347G>C
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ENSP00000496133.1:p.Gly116Ala
|
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ENST00000645285.1:c.158G>C
|
ENSP00000495058.1:p.Gly53Ala
|
|
ENST00000645331.1:n.1839G>C
|
|
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ENST00000645620.1:c.347G>C
|
ENSP00000493657.1:p.Gly116Ala
|
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ENST00000646691.1:n.409G>C
|
|
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ENST00000646777.1:n.1409G>C
|
|
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ENST00000647016.1:n.1556G>C
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|
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ENST00000647152.1:c.347G>C
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ENSP00000495893.1:p.Gly116Ala
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ENST00000647209.1:c.*945G>C
|
ENSP00000495558.1:n.*945G>C
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ENST00000647346.1:n.2096G>C
|
|
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ENST00000299427.10:c.1076G>C
|
ENSP00000299427.6:p.Gly359Ala
|
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ENST00000524924.1:n.31G>C
|
|
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ENST00000533371.5:c.347G>C
|
ENSP00000437066.1:p.Gly116Ala
|
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ENST00000611494.4:c.1076G>C
|
ENSP00000484546.1:p.Gly359Ala
|
|
NM_000391.3:c.1076G>C
|
NP_000382.3:p.Gly359Ala
|
|
NM_000391.4:c.1076G>C
MANE Select
|
NP_000382.3:p.Gly359Ala
|
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