ENST00000593677.2:c.1957+779A>G
|
|
|
ENST00000688602.1:c.3385A>G
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|
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ENST00000689936.1:c.3357A>G
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|
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ENST00000692547.1:n.445A>G
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|
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ENST00000359596.8:c.15052A>G
MANE Select
|
ENSP00000352608.2:p.Arg5018Gly
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ENST00000355481.8:c.15037A>G
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ENSP00000347667.3:p.Arg5013Gly
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|
ENST00000359596.7:c.15052A>G
|
ENSP00000352608.2:p.Arg5018Gly
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|
ENST00000360985.7:c.15034A>G
|
ENSP00000354254.4:p.Arg5012Gly
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NM_000540.2:c.15052A>G , LRG_766t1:c.15052A>G
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NP_000531.2:p.Arg5018Gly
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NM_001042723.1:c.15037A>G
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NP_001036188.1:p.Arg5013Gly
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|
XM_006723317.1:c.15034A>G
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XP_006723380.1:p.Arg5012Gly
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|
XM_006723319.1:c.15019A>G
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XP_006723382.1:p.Arg5007Gly
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|
XM_011527204.1:c.15049A>G
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XP_011525506.1:p.Arg5017Gly
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|
XM_011527205.1:c.14965A>G
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XP_011525507.1:p.Arg4989Gly
|
|
XM_006723317.2:c.15034A>G
|
XP_006723380.1:p.Arg5012Gly
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|
XM_006723319.2:c.15019A>G
|
XP_006723382.1:p.Arg5007Gly
|
|
XM_011527205.2:c.14965A>G
|
XP_011525507.1:p.Arg4989Gly
|
|
NM_000540.3:c.15052A>G
MANE Select
|
NP_000531.2:p.Arg5018Gly
|
|
NM_001042723.2:c.15037A>G
|
NP_001036188.1:p.Arg5013Gly
|
|