ENST00000355699.7:c.2858C>T
MANE Select
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ENSP00000347927.2:p.Ala953Val
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ENST00000355699.6:c.2858C>T
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ENSP00000347927.2:p.Ala953Val
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ENST00000356589.6:c.2765C>T
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ENSP00000348997.2:p.Ala922Val
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ENST00000371916.5:c.*327C>T
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ENSP00000360984.2:n.*327C>T
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ENST00000371929.7:c.2858C>T
|
ENSP00000360997.3:p.Ala953Val
|
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ENST00000485925.5:n.1674C>T
|
|
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ENST00000495234.5:c.*1690C>T
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ENSP00000435274.1:n.*1690C>T
|
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NM_139025.4:c.2858C>T , LRG_544t1:c.2858C>T
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NP_620594.1:p.Ala953Val
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NM_139026.4:c.2765C>T
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NP_620595.1:p.Ala922Val
|
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NM_139027.4:c.2858C>T
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NP_620596.2:p.Ala953Val
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NR_024514.2:n.1693C>T
|
|
|
XM_011518174.1:c.2468C>T
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XP_011516476.1:p.Ala823Val
|
|
XM_011518175.1:c.2858C>T
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XP_011516477.1:p.Ala953Val
|
|
XM_011518176.1:c.1874C>T
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XP_011516478.1:p.Ala625Val
|
|
XM_011518177.1:c.1868C>T
|
XP_011516479.1:p.Ala623Val
|
|
XM_011518178.1:c.1523C>T
|
XP_011516480.1:p.Ala508Val
|
|
XM_011518179.1:c.1523C>T
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XP_011516481.1:p.Ala508Val
|
|
XM_011518180.1:c.1124C>T
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XP_011516482.1:p.Ala375Val
|
|
XM_011518176.3:c.1874C>T
|
XP_011516478.1:p.Ala625Val
|
|
XM_011518178.2:c.1523C>T
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XP_011516480.1:p.Ala508Val
|
|
XM_017014232.1:c.2846C>T
|
XP_016869721.1:p.Ala949Val
|
|
XM_017014233.1:c.2468C>T
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XP_016869722.1:p.Ala823Val
|
|
XM_017014234.2:c.1868C>T
|
XP_016869723.1:p.Ala623Val
|
|
XR_001746171.1:n.3631C>T
|
|
|
NM_139026.5:c.2765C>T
|
NP_620595.1:p.Ala922Val
|
|
NM_139027.5:c.2858C>T
|
NP_620596.2:p.Ala953Val
|
|
NM_139025.5:c.2858C>T
|
NP_620594.1:p.Ala953Val
|
|
NM_139026.6:c.2765C>T
|
NP_620595.1:p.Ala922Val
|
|
NM_139027.6:c.2858C>T
MANE Select
|
NP_620596.2:p.Ala953Val
|
|
NR_024514.3:n.1695C>T
|
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