ENST00000372811.10:c.541T>A
MANE Select
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ENSP00000361898.6:p.Ser181Thr
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ENST00000372809.5:c.580T>A
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ENSP00000361895.5:p.Ser194Thr
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ENST00000372811.9:c.541T>A
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ENSP00000361898.5:p.Ser181Thr
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ENST00000420632.6:c.73T>A
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ENSP00000391261.2:p.Ser25Thr
|
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ENST00000434861.5:c.535T>A
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ENSP00000407606.1:p.Ser179Thr
|
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ENST00000469745.5:n.453T>A
|
|
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ENST00000480630.5:n.1188T>A
|
|
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ENST00000483824.5:n.676T>A
|
|
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NM_001136493.2:c.580T>A
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NP_001129965.1:p.Ser194Thr
|
|
NM_001287808.1:c.73T>A
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NP_001274737.1:p.Ser25Thr
|
|
NM_001287809.1:c.430T>A
|
NP_001274738.1:p.Ser144Thr
|
|
NM_032793.4:c.541T>A
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NP_116182.2:p.Ser181Thr
|
|
NR_109896.1:n.722T>A
|
|
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XM_005271285.1:c.535T>A
|
XP_005271342.1:p.Ser179Thr
|
|
XM_011542312.1:c.541T>A
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XP_011540614.1:p.Ser181Thr
|
|
XR_946783.1:n.689T>A
|
|
|
NM_001349821.1:c.535T>A
|
NP_001336750.1:p.Ser179Thr
|
|
NM_001349822.1:c.541T>A
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NP_001336751.1:p.Ser181Thr
|
|
NM_001349823.1:c.196T>A
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NP_001336752.1:p.Ser66Thr
|
|
NM_001136493.3:c.580T>A
|
NP_001129965.1:p.Ser194Thr
|
|
NM_001287809.2:c.430T>A
|
NP_001274738.1:p.Ser144Thr
|
|
NM_001349821.2:c.535T>A
|
NP_001336750.1:p.Ser179Thr
|
|
NM_001349822.2:c.541T>A
|
NP_001336751.1:p.Ser181Thr
|
|
NM_001349823.2:c.196T>A
|
NP_001336752.1:p.Ser66Thr
|
|
NM_032793.5:c.541T>A
MANE Select
|
NP_116182.2:p.Ser181Thr
|
|
NR_109896.2:n.689T>A
|
|
|
NM_001287808.2:c.73T>A
|
NP_001274737.1:p.Ser25Thr
|
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