ENST00000593677.2:c.1583T>G
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ENST00000688602.1:c.2980T>G
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ENST00000689936.1:c.2952T>G
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ENST00000692547.1:n.40T>G
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ENST00000359596.8:c.14647T>G
MANE Select
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ENSP00000352608.2:p.Cys4883Gly
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ENST00000355481.8:c.14632T>G
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ENSP00000347667.3:p.Cys4878Gly
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ENST00000359596.7:c.14647T>G
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ENSP00000352608.2:p.Cys4883Gly
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ENST00000360985.7:c.14629T>G
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ENSP00000354254.4:p.Cys4877Gly
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NM_000540.2:c.14647T>G , LRG_766t1:c.14647T>G
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NP_000531.2:p.Cys4883Gly
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NM_001042723.1:c.14632T>G
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NP_001036188.1:p.Cys4878Gly
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XM_006723317.1:c.14629T>G
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XP_006723380.1:p.Cys4877Gly
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XM_006723319.1:c.14614T>G
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XP_006723382.1:p.Cys4872Gly
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XM_011527204.1:c.14644T>G
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XP_011525506.1:p.Cys4882Gly
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|
XM_011527205.1:c.14560T>G
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XP_011525507.1:p.Cys4854Gly
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|
XM_006723317.2:c.14629T>G
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XP_006723380.1:p.Cys4877Gly
|
|
XM_006723319.2:c.14614T>G
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XP_006723382.1:p.Cys4872Gly
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XM_011527205.2:c.14560T>G
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XP_011525507.1:p.Cys4854Gly
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NM_000540.3:c.14647T>G
MANE Select
|
NP_000531.2:p.Cys4883Gly
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|
NM_001042723.2:c.14632T>G
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NP_001036188.1:p.Cys4878Gly
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