ENST00000258385.8:c.1302G>A
MANE Select
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ENSP00000258385.3:p.Glu434=
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ENST00000258385.7:c.1302G>A
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ENSP00000258385.3:p.Glu434=
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ENST00000441621.6:c.*484G>A
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ENSP00000408819.2:n.*484G>A
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ENST00000446616.1:c.*943G>A
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ENSP00000410801.1:n.*943G>A
|
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ENST00000543200.5:c.1257G>A
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ENSP00000438380.1:p.Glu419=
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NM_000751.2:c.1302G>A
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NP_000742.1:p.Glu434=
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NM_001256657.1:c.1257G>A
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NP_001243586.1:p.Glu419=
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NM_001311195.1:c.720G>A
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NP_001298124.1:p.Glu240=
|
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NM_001311196.1:c.999G>A
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NP_001298125.1:p.Glu333=
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NR_046333.1:c.-4294966249G>A
|
|
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NR_046334.1:c.-4294965970G>A
|
|
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XM_011510524.1:c.921G>A
|
XP_011508826.1:p.Glu307=
|
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XM_011510524.2:c.921G>A
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XP_011508826.1:p.Glu307=
|
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NM_000751.3:c.1302G>A
MANE Select
|
NP_000742.1:p.Glu434=
|
|
NM_001311195.2:c.720G>A
|
NP_001298124.1:p.Glu240=
|
|
NM_001311196.2:c.999G>A
|
NP_001298125.1:p.Glu333=
|
|
NM_001256657.2:c.1257G>A
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NP_001243586.1:p.Glu419=
|
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