ENST00000240651.14:c.317T>C
MANE Select
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ENSP00000240651.9:p.Val106Ala
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ENST00000240651.13:c.317T>C
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ENSP00000240651.9:p.Val106Ala
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ENST00000375266.8:c.*243T>C
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ENSP00000364415.4:n.*243T>C
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ENST00000538582.5:c.104T>C
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ENSP00000438505.1:p.Val35Ala
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ENST00000543476.5:c.317T>C
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ENSP00000440192.1:p.Val106Ala
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ENST00000544970.5:c.317T>C
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ENSP00000439106.1:p.Val106Ala
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NM_024854.3:c.317T>C
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NP_079130.2:p.Val106Ala
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XM_006719153.2:c.317T>C
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XP_006719216.1:p.Val106Ala
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XR_242902.3:n.444T>C
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NM_001350912.1:c.104T>C
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NP_001337841.1:p.Val35Ala
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NM_001350913.1:c.-387T>C
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NP_001337842.1:n.-387T>C
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NM_024854.4:c.317T>C
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NP_079130.2:p.Val106Ala
|
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XM_006719153.3:c.317T>C
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XP_006719216.1:p.Val106Ala
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XR_242902.4:n.418T>C
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|
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NM_024854.5:c.317T>C
MANE Select
|
NP_079130.2:p.Val106Ala
|
|
NM_001350913.2:c.-387T>C
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NP_001337842.1:n.-387T>C
|
|
NM_001350912.2:c.104T>C
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NP_001337841.1:p.Val35Ala
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