ENST00000258385.8:c.1218G>A
MANE Select
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ENSP00000258385.3:p.Glu406=
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ENST00000258385.7:c.1218G>A
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ENSP00000258385.3:p.Glu406=
|
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ENST00000441621.6:c.*400G>A
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ENSP00000408819.2:n.*400G>A
|
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ENST00000446616.1:c.*859G>A
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ENSP00000410801.1:n.*859G>A
|
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ENST00000543200.5:c.1173G>A
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ENSP00000438380.1:p.Glu391=
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NM_000751.2:c.1218G>A
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NP_000742.1:p.Glu406=
|
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NM_001256657.1:c.1173G>A
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NP_001243586.1:p.Glu391=
|
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NM_001311195.1:c.636G>A
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NP_001298124.1:p.Glu212=
|
|
NM_001311196.1:c.915G>A
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NP_001298125.1:p.Glu305=
|
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NR_046333.1:c.-4294966333G>A
|
|
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NR_046334.1:c.-4294966054G>A
|
|
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XM_011510524.1:c.837G>A
|
XP_011508826.1:p.Glu279=
|
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XM_011510524.2:c.837G>A
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XP_011508826.1:p.Glu279=
|
|
NM_000751.3:c.1218G>A
MANE Select
|
NP_000742.1:p.Glu406=
|
|
NM_001311195.2:c.636G>A
|
NP_001298124.1:p.Glu212=
|
|
NM_001311196.2:c.915G>A
|
NP_001298125.1:p.Glu305=
|
|
NM_001256657.2:c.1173G>A
|
NP_001243586.1:p.Glu391=
|
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