ENST00000688602.1:c.1288C>G
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ENST00000689936.1:c.1270C>G
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ENST00000359596.8:c.12878C>G
MANE Select
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ENSP00000352608.2:p.Ala4293Gly
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ENST00000355481.8:c.12863C>G
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ENSP00000347667.3:p.Ala4288Gly
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ENST00000359596.7:c.12878C>G
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ENSP00000352608.2:p.Ala4293Gly
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ENST00000360985.7:c.12860C>G
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ENSP00000354254.4:p.Ala4287Gly
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ENST00000594335.5:c.6247C>G
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NM_000540.2:c.12878C>G , LRG_766t1:c.12878C>G
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NP_000531.2:p.Ala4293Gly
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NM_001042723.1:c.12863C>G
|
NP_001036188.1:p.Ala4288Gly
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XM_006723317.1:c.12860C>G
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XP_006723380.1:p.Ala4287Gly
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XM_006723319.1:c.12845C>G
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XP_006723382.1:p.Ala4282Gly
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XM_011527204.1:c.12875C>G
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XP_011525506.1:p.Ala4292Gly
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|
XM_011527205.1:c.12878C>G
|
XP_011525507.1:p.Ala4293Gly
|
|
XM_006723317.2:c.12860C>G
|
XP_006723380.1:p.Ala4287Gly
|
|
XM_006723319.2:c.12845C>G
|
XP_006723382.1:p.Ala4282Gly
|
|
XM_011527205.2:c.12878C>G
|
XP_011525507.1:p.Ala4293Gly
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NM_000540.3:c.12878C>G
MANE Select
|
NP_000531.2:p.Ala4293Gly
|
|
NM_001042723.2:c.12863C>G
|
NP_001036188.1:p.Ala4288Gly
|
|