ENST00000233627.14:c.379A=
MANE Select
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ENSP00000233627.9:p.Thr127=
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ENST00000233627.13:c.379A=
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ENSP00000233627.9:p.Thr127=
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|
ENST00000313408.11:c.379A=
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ENSP00000364262.5:p.Thr127=
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ENST00000414651.3:c.469A=
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ENSP00000406630.2:p.Thr157=
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ENST00000436115.6:n.2334A=
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ENST00000534853.5:c.*173A=
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ENSP00000442822.1:n.*173A=
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ENST00000535382.1:n.631A=
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|
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ENST00000538523.5:n.435A=
|
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ENST00000538662.5:n.406A=
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ENST00000538929.5:n.469A=
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|
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ENST00000539480.5:c.379A=
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ENSP00000443273.1:p.Thr127=
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|
ENST00000540530.5:n.370A=
|
|
|
ENST00000543289.5:n.869A=
|
|
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ENST00000545446.5:n.670A=
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ENST00000546172.7:c.*375A=
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ENSP00000467094.1:n.*375A=
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|
ENST00000546283.5:c.379A=
|
ENSP00000440348.1:p.Thr127=
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|
ENST00000618074.4:c.379A=
|
ENSP00000477895.1:p.Thr127=
|
|
ENST00000620479.4:c.379A=
|
ENSP00000480984.1:p.Thr127=
|
|
ENST00000622587.4:n.375A=
|
|
|
NM_024407.4:c.379A=
|
NP_077718.3:p.Thr127=
|
|
XM_005259556.3:c.379A=
|
XP_005259613.2:p.Thr127=
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|
NM_001363602.1:c.379A=
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NP_001350531.1:p.Thr127=
|
|
XM_024451499.1:c.400A=
|
XP_024307267.1:p.Thr134=
|
|
NM_024407.5:c.379A=
MANE Select
|
NP_077718.3:p.Thr127=
|
|
NM_001363602.2:c.379A=
|
NP_001350531.1:p.Thr127=
|
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