ENST00000403733.8:c.3257A>C
MANE Select
|
ENSP00000384222.3:p.Glu1086Ala
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ENST00000403733.7:c.3257A>C
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ENSP00000384222.3:p.Glu1086Ala
|
|
ENST00000427431.5:c.*2649A>C
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ENSP00000393342.1:n.*2649A>C
|
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ENST00000438543.5:c.*1053A>C
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ENSP00000413521.1:n.*1053A>C
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ENST00000448232.6:c.3329A>C
|
ENSP00000398577.2:p.Glu1110Ala
|
|
ENST00000504005.5:c.2303A>C
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ENSP00000427569.1:p.Glu768Ala
|
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ENST00000508747.1:c.641A>C
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ENSP00000420835.1:p.Glu214Ala
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ENST00000513834.5:c.3110A>C
|
ENSP00000425054.1:p.Glu1037Ala
|
|
NM_024949.5:c.3257A>C
|
NP_079225.5:p.Glu1086Ala
|
|
XM_011532269.1:c.3329A>C
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XP_011530571.1:p.Glu1110Ala
|
|
XM_011532269.3:c.3329A>C
|
XP_011530571.1:p.Glu1110Ala
|
|
XM_024454225.1:c.3035A>C
|
XP_024309993.1:p.Glu1012Ala
|
|
NM_024949.6:c.3257A>C
MANE Select
|
NP_079225.5:p.Glu1086Ala
|
|