ENST00000236671.7:c.995T>C
MANE Select
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ENSP00000236671.2:p.Val332Ala
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ENST00000367196.4:c.890T>C
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ENSP00000356164.4:p.Val297Ala
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ENST00000427721.3:c.420T>C
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|
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ENST00000429746.2:c.890T>C
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ENSP00000402586.2:p.Val297Ala
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ENST00000433655.6:c.*161T>C
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ENSP00000404902.1:n.*161T>C
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ENST00000438213.6:c.1112T>C
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ENSP00000415036.2:p.Val371Ala
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ENST00000497544.3:n.703T>C
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|
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ENST00000636397.1:c.995T>C
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ENSP00000489910.1:p.Val332Ala
|
|
ENST00000636571.1:c.974T>C
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ENSP00000490770.1:p.Val325Ala
|
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ENST00000636615.1:c.995T>C
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ENSP00000490014.1:p.Val332Ala
|
|
ENST00000636843.1:c.989T>C
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ENSP00000490897.1:p.Val330Ala
|
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ENST00000637158.1:n.593T>C
|
|
|
ENST00000637381.2:n.3423T>C
|
|
|
ENST00000637387.1:c.974T>C
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ENSP00000490598.1:p.Val325Ala
|
|
ENST00000637815.2:c.977T>C
|
ENSP00000490344.1:p.Val326Ala
|
|
ENST00000637915.1:c.995T>C
|
ENSP00000490471.1:p.Val332Ala
|
|
ENST00000637937.1:n.303T>C
|
|
|
ENST00000678991.1:c.*856T>C
|
ENSP00000503019.1:n.*856T>C
|
|
ENST00000236671.6:c.995T>C
|
ENSP00000236671.2:p.Val332Ala
|
|
ENST00000427721.2:c.395T>C
|
ENSP00000415840.2:p.Val132Ala
|
|
ENST00000429746.1:c.326T>C
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ENSP00000402586.1:p.Val109Ala
|
|
ENST00000433655.5:c.*161T>C
|
ENSP00000404902.1:n.*161T>C
|
|
ENST00000497544.1:n.703T>C
|
|
|
NM_001909.4:c.995T>C
|
NP_001900.1:p.Val332Ala
|
|
NM_001909.5:c.995T>C
MANE Select
|
NP_001900.1:p.Val332Ala
|
|