ENST00000236671.7:c.1030G>T
MANE Select
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ENSP00000236671.2:p.Gly344Cys
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ENST00000367196.4:c.925G>T
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ENSP00000356164.4:p.Gly309Cys
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ENST00000427721.3:c.455G>T
|
|
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ENST00000429746.2:c.925G>T
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ENSP00000402586.2:p.Gly309Cys
|
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ENST00000433655.6:c.*196G>T
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ENSP00000404902.1:n.*196G>T
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|
ENST00000438213.6:c.1147G>T
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ENSP00000415036.2:p.Gly383Cys
|
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ENST00000497544.3:n.738G>T
|
|
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ENST00000636397.1:c.1030G>T
|
ENSP00000489910.1:p.Gly344Cys
|
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ENST00000636571.1:c.1009G>T
|
ENSP00000490770.1:p.Gly337Cys
|
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ENST00000636579.1:c.31G>T
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ENSP00000490489.1:p.Gly11Cys
|
|
ENST00000636615.1:c.1030G>T
|
ENSP00000490014.1:p.Gly344Cys
|
|
ENST00000636843.1:c.1024G>T
|
ENSP00000490897.1:p.Gly342Cys
|
|
ENST00000637158.1:n.628G>T
|
|
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ENST00000637381.2:n.3458G>T
|
|
|
ENST00000637387.1:c.1009G>T
|
ENSP00000490598.1:p.Gly337Cys
|
|
ENST00000637815.2:c.1012G>T
|
ENSP00000490344.1:p.Gly338Cys
|
|
ENST00000637915.1:c.1030G>T
|
ENSP00000490471.1:p.Gly344Cys
|
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ENST00000637937.1:n.338G>T
|
|
|
ENST00000678991.1:c.*891G>T
|
ENSP00000503019.1:n.*891G>T
|
|
ENST00000236671.6:c.1030G>T
|
ENSP00000236671.2:p.Gly344Cys
|
|
ENST00000427721.2:c.430G>T
|
ENSP00000415840.2:p.Gly144Cys
|
|
ENST00000429746.1:c.361G>T
|
ENSP00000402586.1:p.Gly121Cys
|
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ENST00000433655.5:c.*196G>T
|
ENSP00000404902.1:n.*196G>T
|
|
ENST00000497544.1:n.738G>T
|
|
|
NM_001909.4:c.1030G>T
|
NP_001900.1:p.Gly344Cys
|
|
NM_001909.5:c.1030G>T
MANE Select
|
NP_001900.1:p.Gly344Cys
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