ENST00000593677.2:c.1627C>A
|
|
|
ENST00000688602.1:c.3024C>A
|
|
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ENST00000689936.1:c.2996C>A
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|
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ENST00000692547.1:n.84C>A
|
|
|
ENST00000359596.8:c.14691C>A
MANE Select
|
ENSP00000352608.2:p.Gly4897=
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|
ENST00000355481.8:c.14676C>A
|
ENSP00000347667.3:p.Gly4892=
|
|
ENST00000359596.7:c.14691C>A
|
ENSP00000352608.2:p.Gly4897=
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|
ENST00000360985.7:c.14673C>A
|
ENSP00000354254.4:p.Gly4891=
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NM_000540.2:c.14691C>A , LRG_766t1:c.14691C>A
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NP_000531.2:p.Gly4897=
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|
NM_001042723.1:c.14676C>A
|
NP_001036188.1:p.Gly4892=
|
|
XM_006723317.1:c.14673C>A
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XP_006723380.1:p.Gly4891=
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|
XM_006723319.1:c.14658C>A
|
XP_006723382.1:p.Gly4886=
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|
XM_011527204.1:c.14688C>A
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XP_011525506.1:p.Gly4896=
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|
XM_011527205.1:c.14604C>A
|
XP_011525507.1:p.Gly4868=
|
|
XM_006723317.2:c.14673C>A
|
XP_006723380.1:p.Gly4891=
|
|
XM_006723319.2:c.14658C>A
|
XP_006723382.1:p.Gly4886=
|
|
XM_011527205.2:c.14604C>A
|
XP_011525507.1:p.Gly4868=
|
|
NM_000540.3:c.14691C>A
MANE Select
|
NP_000531.2:p.Gly4897=
|
|
NM_001042723.2:c.14676C>A
|
NP_001036188.1:p.Gly4892=
|
|