ENST00000541682.7:c.232G>A
MANE Select
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ENSP00000446205.2:p.Ala78Thr
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ENST00000317814.8:c.227-10G>A
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ENSP00000314774.4:n.227-10G>A
|
|
ENST00000541682.6:c.232G>A
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ENSP00000446205.2:p.Ala78Thr
|
|
ENST00000577735.1:c.208G>A
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ENSP00000462491.1:p.Ala70Thr
|
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NM_001165967.1:c.232G>A
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NP_001159439.1:p.Ala78Thr
|
|
NM_032580.3:c.227-10G>A
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NP_115969.2:n.227-10G>A
|
|
XM_011524038.1:c.337G>A
|
XP_011522340.1:p.Ala113Thr
|
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XM_011524039.1:c.328G>A
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XP_011522341.1:p.Ala110Thr
|
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XM_011524040.1:c.328G>A
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XP_011522342.1:p.Ala110Thr
|
|
XM_011524041.1:c.319G>A
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XP_011522343.1:p.Ala107Thr
|
|
XM_011524042.1:c.190G>A
|
XP_011522344.1:p.Ala64Thr
|
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XR_934203.1:n.69+2218C>T
|
|
|
XM_017025232.1:c.337G>A
|
XP_016880721.1:p.Ala113Thr
|
|
XM_024451007.1:c.337G>A
|
XP_024306775.1:p.Ala113Thr
|
|
NM_001165967.2:c.232G>A
MANE Select
|
NP_001159439.1:p.Ala78Thr
|
|
NM_032580.4:c.227-10G>A
|
NP_115969.2:n.227-10G>A
|
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