ENST00000253122.10:c.1367T>C
MANE Select
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ENSP00000253122.5:p.Val456Ala
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ENST00000253122.9:c.1367T>C
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ENSP00000253122.5:p.Val456Ala
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ENST00000413787.1:c.296T>C
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ENSP00000400463.1:p.Val99Ala
|
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ENST00000430077.6:c.1022T>C
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ENSP00000403041.2:p.Val341Ala
|
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ENST00000442457.1:c.421T>C
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|
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ENST00000485324.1:n.1512T>C
|
|
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NM_001142805.1:c.1337T>C
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NP_001136277.1:p.Val446Ala
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NM_001142806.1:c.1022T>C
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NP_001136278.1:p.Val341Ala
|
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NM_005629.3:c.1367T>C
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NP_005620.1:p.Val456Ala
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NM_005629.4:c.1367T>C
MANE Select
|
NP_005620.1:p.Val456Ala
|
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NM_001142805.2:c.1337T>C
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NP_001136277.1:p.Val446Ala
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