ENST00000593677.2:c.1644A>T
|
|
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ENST00000688602.1:c.3041A>T
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|
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ENST00000689936.1:c.3013A>T
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|
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ENST00000692547.1:n.101A>T
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|
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ENST00000359596.8:c.14708A>T
MANE Select
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ENSP00000352608.2:p.Glu4903Val
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ENST00000355481.8:c.14693A>T
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ENSP00000347667.3:p.Glu4898Val
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|
ENST00000359596.7:c.14708A>T
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ENSP00000352608.2:p.Glu4903Val
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|
ENST00000360985.7:c.14690A>T
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ENSP00000354254.4:p.Glu4897Val
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NM_000540.2:c.14708A>T , LRG_766t1:c.14708A>T
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NP_000531.2:p.Glu4903Val
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NM_001042723.1:c.14693A>T
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NP_001036188.1:p.Glu4898Val
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|
XM_006723317.1:c.14690A>T
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XP_006723380.1:p.Glu4897Val
|
|
XM_006723319.1:c.14675A>T
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XP_006723382.1:p.Glu4892Val
|
|
XM_011527204.1:c.14705A>T
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XP_011525506.1:p.Glu4902Val
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|
XM_011527205.1:c.14621A>T
|
XP_011525507.1:p.Glu4874Val
|
|
XM_006723317.2:c.14690A>T
|
XP_006723380.1:p.Glu4897Val
|
|
XM_006723319.2:c.14675A>T
|
XP_006723382.1:p.Glu4892Val
|
|
XM_011527205.2:c.14621A>T
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XP_011525507.1:p.Glu4874Val
|
|
NM_000540.3:c.14708A>T
MANE Select
|
NP_000531.2:p.Glu4903Val
|
|
NM_001042723.2:c.14693A>T
|
NP_001036188.1:p.Glu4898Val
|
|