ENST00000218099.7:c.398C>A
MANE Select
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ENSP00000218099.2:p.Thr133Lys
|
|
ENST00000643157.1:n.1065C>A
|
|
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ENST00000218099.6:c.398C>A
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ENSP00000218099.2:p.Thr133Lys
|
|
ENST00000394090.2:c.284C>A
|
ENSP00000377650.2:p.Thr95Lys
|
|
ENST00000479617.2:n.351C>A
|
|
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NM_000133.3:c.398C>A , LRG_556t1:c.398C>A
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NP_000124.1:p.Thr133Lys
|
|
NM_001313913.1:c.284C>A
|
NP_001300842.1:p.Thr95Lys
|
|
XM_005262397.3:c.392-2693C>A
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XP_005262454.1:n.392-2693C>A
|
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XM_005262397.4:c.392-2693C>A
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XP_005262454.1:n.392-2693C>A
|
|
NM_000133.4:c.398C>A
MANE Select
|
NP_000124.1:p.Thr133Lys
|
|
NM_001313913.2:c.284C>A
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NP_001300842.1:p.Thr95Lys
|
|