ENST00000409350.6:c.248A>C
|
ENSP00000386968.2:p.Asp83Ala
|
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ENST00000439384.6:n.471A>C
|
|
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ENST00000446446.6:c.209A>C
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ENSP00000396867.2:p.Asp70Ala
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ENST00000706158.1:c.*153A>C
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ENSP00000516236.1:n.*153A>C
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ENST00000706159.1:c.121A>C
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ENSP00000516237.1:p.Met41Leu
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ENST00000706160.1:c.209A>C
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ENSP00000516238.1:p.Asp70Ala
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ENST00000706161.1:c.287A>C
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ENSP00000516239.1:p.Asp96Ala
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ENST00000706162.1:c.209A>C
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ENSP00000516240.1:p.Asp70Ala
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ENST00000706163.1:c.50-81874A>C
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ENSP00000516241.1:n.50-81874A>C
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ENST00000222792.11:c.209A>C
MANE Select
|
ENSP00000222792.7:p.Asp70Ala
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ENST00000644824.1:c.434A>C
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ENSP00000495614.1:p.Asp145Ala
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ENST00000222792.10:c.209A>C
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ENSP00000222792.6:p.Asp70Ala
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ENST00000409350.5:c.248A>C
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ENSP00000386968.1:p.Asp83Ala
|
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ENST00000409922.5:n.420A>C
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|
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ENST00000409964.6:n.408A>C
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|
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ENST00000412536.5:n.229A>C
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|
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ENST00000435288.6:c.168+4703A>C
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ENSP00000400282.3:n.168+4703A>C
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|
ENST00000439384.5:c.434A>C
|
ENSP00000409843.1:p.Asp145Ala
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ENST00000474070.5:c.309A>C
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|
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ENST00000478128.6:n.303A>C
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|
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ENST00000482820.6:n.418A>C
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|
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ENST00000491856.1:n.1758A>C
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|
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ENST00000495789.6:c.209A>C
|
ENSP00000438587.2:p.Asp70Ala
|
|
ENST00000539389.5:c.209A>C
|
ENSP00000440526.2:p.Asp70Ala
|
|
ENST00000539406.5:c.209A>C
|
ENSP00000444063.2:p.Asp70Ala
|
|
NM_001293069.1:c.434A>C
|
NP_001279998.1:p.Asp145Ala
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|
NM_001293070.1:c.248A>C
|
NP_001279999.1:p.Asp83Ala
|
|
NM_001293071.1:c.104A>C
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NP_001280000.1:p.Asp35Ala
|
|
NM_001293072.1:c.164A>C
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NP_001280001.1:p.Asp55Ala
|
|
NM_004067.3:c.209A>C
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NP_004058.1:p.Asp70Ala
|
|
XM_011515105.1:c.512A>C
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XP_011513407.1:p.Asp171Ala
|
|
XM_011515106.1:c.473A>C
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XP_011513408.1:p.Asp158Ala
|
|
XM_011515107.1:c.287A>C
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XP_011513409.1:p.Asp96Ala
|
|
XM_011515108.1:c.209A>C
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XP_011513410.1:p.Asp70Ala
|
|
XM_011515109.1:c.170A>C
|
XP_011513411.1:p.Asp57Ala
|
|
XM_011515110.1:c.131A>C
|
XP_011513412.1:p.Asp44Ala
|
|
XM_011515111.1:c.104A>C
|
XP_011513413.1:p.Asp35Ala
|
|
XM_011515112.1:c.512A>C
|
XP_011513414.1:p.Asp171Ala
|
|
XM_011515105.2:c.512A>C
|
XP_011513407.1:p.Asp171Ala
|
|
XM_011515106.2:c.473A>C
|
XP_011513408.1:p.Asp158Ala
|
|
XM_011515107.2:c.287A>C
|
XP_011513409.1:p.Asp96Ala
|
|
XM_017011721.1:c.530A>C
|
XP_016867210.1:p.Asp177Ala
|
|
XM_017011722.1:c.305A>C
|
XP_016867211.1:p.Asp102Ala
|
|
NM_004067.4:c.209A>C
MANE Select
|
NP_004058.1:p.Asp70Ala
|
|
NM_001293070.2:c.248A>C
|
NP_001279999.1:p.Asp83Ala
|
|
NM_001293071.2:c.104A>C
|
NP_001280000.1:p.Asp35Ala
|
|
NM_001293072.2:c.164A>C
|
NP_001280001.1:p.Asp55Ala
|
|
NM_001398427.1:c.-230A>C
|
NP_001385356.1:n.-230A>C
|
|