ENST00000593677.2:c.993G>C
|
|
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ENST00000688602.1:c.2390G>C
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|
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ENST00000689936.1:c.2362G>C
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|
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ENST00000359596.8:c.14057G>C
MANE Select
|
ENSP00000352608.2:p.Gly4686Ala
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ENST00000355481.8:c.14042G>C
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ENSP00000347667.3:p.Gly4681Ala
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|
ENST00000359596.7:c.14057G>C
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ENSP00000352608.2:p.Gly4686Ala
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ENST00000360985.7:c.14039G>C
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ENSP00000354254.4:p.Gly4680Ala
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NM_000540.2:c.14057G>C , LRG_766t1:c.14057G>C
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NP_000531.2:p.Gly4686Ala
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NM_001042723.1:c.14042G>C
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NP_001036188.1:p.Gly4681Ala
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|
XM_006723317.1:c.14039G>C
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XP_006723380.1:p.Gly4680Ala
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|
XM_006723319.1:c.14024G>C
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XP_006723382.1:p.Gly4675Ala
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XM_011527204.1:c.14054G>C
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XP_011525506.1:p.Gly4685Ala
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|
XM_011527205.1:c.13970G>C
|
XP_011525507.1:p.Gly4657Ala
|
|
XM_006723317.2:c.14039G>C
|
XP_006723380.1:p.Gly4680Ala
|
|
XM_006723319.2:c.14024G>C
|
XP_006723382.1:p.Gly4675Ala
|
|
XM_011527205.2:c.13970G>C
|
XP_011525507.1:p.Gly4657Ala
|
|
NM_000540.3:c.14057G>C
MANE Select
|
NP_000531.2:p.Gly4686Ala
|
|
NM_001042723.2:c.14042G>C
|
NP_001036188.1:p.Gly4681Ala
|
|