ENST00000181839.10:c.2109T>A
MANE Select
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ENSP00000181839.4:p.Asp703Glu
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ENST00000340829.10:c.2109T>A
|
ENSP00000340557.5:p.Asp703Glu
|
|
ENST00000484589.2:c.661T>A
|
|
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ENST00000642213.1:n.591T>A
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|
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ENST00000643859.1:c.1000T>A
|
|
|
ENST00000643915.1:c.423T>A
|
ENSP00000496187.1:p.Asp141Glu
|
|
ENST00000645470.1:c.39T>A
|
ENSP00000495036.1:p.Asp13Glu
|
|
ENST00000646039.1:c.1449T>A
|
ENSP00000494168.1:p.Asp483Glu
|
|
ENST00000646437.1:c.743T>A
|
|
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ENST00000647453.1:n.1178T>A
|
|
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ENST00000647518.1:n.3946T>A
|
|
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ENST00000181839.8:c.2109T>A
|
ENSP00000181839.4:p.Asp703Glu
|
|
ENST00000340829.9:c.2109T>A
|
ENSP00000340557.5:p.Asp703Glu
|
|
ENST00000484589.1:n.661T>A
|
|
|
ENST00000611390.1:c.267T>A
|
ENSP00000484610.1:p.Asp89Glu
|
|
ENST00000613626.4:c.267T>A
|
ENSP00000480835.1:p.Asp89Glu
|
|
NM_003718.4:c.2109T>A
|
NP_003709.3:p.Asp703Glu
|
|
NM_031267.3:c.2109T>A
|
NP_112557.2:p.Asp703Glu
|
|
XM_011515597.1:c.2109T>A
|
XP_011513899.1:p.Asp703Glu
|
|
XM_011515598.1:c.2109T>A
|
XP_011513900.1:p.Asp703Glu
|
|
XM_011515597.3:c.2109T>A
|
XP_011513899.1:p.Asp703Glu
|
|
XM_017012750.2:c.2109T>A
|
XP_016868239.1:p.Asp703Glu
|
|
XM_017012751.2:c.2109T>A
|
XP_016868240.1:p.Asp703Glu
|
|
NM_003718.5:c.2109T>A
MANE Select
|
NP_003709.3:p.Asp703Glu
|
|