ENST00000218099.7:c.1298A>T
MANE Select
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ENSP00000218099.2:p.Glu433Val
|
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ENST00000643157.1:n.1723+242A>T
|
|
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ENST00000218099.6:c.1298A>T
|
ENSP00000218099.2:p.Glu433Val
|
|
ENST00000394090.2:c.1184A>T
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ENSP00000377650.2:p.Glu395Val
|
|
NM_000133.3:c.1298A>T , LRG_556t1:c.1298A>T
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NP_000124.1:p.Glu433Val
|
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NM_001313913.1:c.1184A>T
|
NP_001300842.1:p.Glu395Val
|
|
XM_005262397.3:c.1169A>T
|
XP_005262454.1:p.Glu390Val
|
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XM_005262397.4:c.1169A>T
|
XP_005262454.1:p.Glu390Val
|
|
NM_000133.4:c.1298A>T
MANE Select
|
NP_000124.1:p.Glu433Val
|
|
NM_001313913.2:c.1184A>T
|
NP_001300842.1:p.Glu395Val
|
|