ENST00000688602.1:c.1237A>C
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|
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ENST00000689936.1:c.1219A>C
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|
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ENST00000359596.8:c.12827A>C
MANE Select
|
ENSP00000352608.2:p.Glu4276Ala
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ENST00000355481.8:c.12812A>C
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ENSP00000347667.3:p.Glu4271Ala
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ENST00000359596.7:c.12827A>C
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ENSP00000352608.2:p.Glu4276Ala
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ENST00000360985.7:c.12809A>C
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ENSP00000354254.4:p.Glu4270Ala
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ENST00000594335.5:c.6196A>C
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NM_000540.2:c.12827A>C , LRG_766t1:c.12827A>C
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NP_000531.2:p.Glu4276Ala
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NM_001042723.1:c.12812A>C
|
NP_001036188.1:p.Glu4271Ala
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|
XM_006723317.1:c.12809A>C
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XP_006723380.1:p.Glu4270Ala
|
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XM_006723319.1:c.12794A>C
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XP_006723382.1:p.Glu4265Ala
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XM_011527204.1:c.12824A>C
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XP_011525506.1:p.Glu4275Ala
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|
XM_011527205.1:c.12827A>C
|
XP_011525507.1:p.Glu4276Ala
|
|
XM_006723317.2:c.12809A>C
|
XP_006723380.1:p.Glu4270Ala
|
|
XM_006723319.2:c.12794A>C
|
XP_006723382.1:p.Glu4265Ala
|
|
XM_011527205.2:c.12827A>C
|
XP_011525507.1:p.Glu4276Ala
|
|
NM_000540.3:c.12827A>C
MANE Select
|
NP_000531.2:p.Glu4276Ala
|
|
NM_001042723.2:c.12812A>C
|
NP_001036188.1:p.Glu4271Ala
|
|