ENST00000541682.7:c.245T>C
MANE Select
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ENSP00000446205.2:p.Val82Ala
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ENST00000317814.8:c.230T>C
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ENSP00000314774.4:p.Val77Ala
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ENST00000541682.6:c.245T>C
|
ENSP00000446205.2:p.Val82Ala
|
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ENST00000577735.1:c.221T>C
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ENSP00000462491.1:p.Val74Ala
|
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NM_001165967.1:c.245T>C
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NP_001159439.1:p.Val82Ala
|
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NM_032580.3:c.230T>C
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NP_115969.2:p.Val77Ala
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XM_011524038.1:c.350T>C
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XP_011522340.1:p.Val117Ala
|
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XM_011524039.1:c.341T>C
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XP_011522341.1:p.Val114Ala
|
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XM_011524040.1:c.341T>C
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XP_011522342.1:p.Val114Ala
|
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XM_011524041.1:c.332T>C
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XP_011522343.1:p.Val111Ala
|
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XM_011524042.1:c.203T>C
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XP_011522344.1:p.Val68Ala
|
|
XR_934203.1:n.69+2205A>G
|
|
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XM_017025232.1:c.350T>C
|
XP_016880721.1:p.Val117Ala
|
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XM_024451007.1:c.350T>C
|
XP_024306775.1:p.Val117Ala
|
|
NM_001165967.2:c.245T>C
MANE Select
|
NP_001159439.1:p.Val82Ala
|
|
NM_032580.4:c.230T>C
|
NP_115969.2:p.Val77Ala
|
|