ENST00000593677.2:c.747C>A
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|
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ENST00000688602.1:c.2144C>A
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|
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ENST00000689936.1:c.2116C>A
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|
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ENST00000359596.8:c.13811C>A
MANE Select
|
ENSP00000352608.2:p.Ala4604Glu
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ENST00000355481.8:c.13796C>A
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ENSP00000347667.3:p.Ala4599Glu
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ENST00000359596.7:c.13811C>A
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ENSP00000352608.2:p.Ala4604Glu
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ENST00000360985.7:c.13793C>A
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ENSP00000354254.4:p.Ala4598Glu
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ENST00000593677.1:c.271C>A
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NM_000540.2:c.13811C>A , LRG_766t1:c.13811C>A
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NP_000531.2:p.Ala4604Glu
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NM_001042723.1:c.13796C>A
|
NP_001036188.1:p.Ala4599Glu
|
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XM_006723317.1:c.13793C>A
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XP_006723380.1:p.Ala4598Glu
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XM_006723319.1:c.13778C>A
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XP_006723382.1:p.Ala4593Glu
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XM_011527204.1:c.13808C>A
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XP_011525506.1:p.Ala4603Glu
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XM_011527205.1:c.13724C>A
|
XP_011525507.1:p.Ala4575Glu
|
|
XM_006723317.2:c.13793C>A
|
XP_006723380.1:p.Ala4598Glu
|
|
XM_006723319.2:c.13778C>A
|
XP_006723382.1:p.Ala4593Glu
|
|
XM_011527205.2:c.13724C>A
|
XP_011525507.1:p.Ala4575Glu
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|
NM_000540.3:c.13811C>A
MANE Select
|
NP_000531.2:p.Ala4604Glu
|
|
NM_001042723.2:c.13796C>A
|
NP_001036188.1:p.Ala4599Glu
|
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