ENST00000211998.10:c.809T=
MANE Select
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ENSP00000211998.5:p.Leu270=
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|
ENST00000211998.8:c.809T=
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ENSP00000211998.4:p.Leu270=
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|
ENST00000372755.7:c.809T=
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ENSP00000361841.3:p.Leu270=
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ENST00000478896.2:n.332-18575T=
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|
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ENST00000623461.3:n.3612T=
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|
|
ENST00000624354.3:c.*564T=
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ENSP00000485551.1:n.*564T=
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|
NM_003373.3:c.809T=
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NP_003364.1:p.Leu270=
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|
NM_014000.2:c.809T= , LRG_383t1:c.809T=
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NP_054706.1:p.Leu270=
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|
XM_005270142.1:c.812T=
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XP_005270199.1:p.Leu271=
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|
XM_005270143.1:c.812T=
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XP_005270200.1:p.Leu271=
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|
XR_001747501.1:n.90-4752A=
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|
|
NM_003373.4:c.809T=
|
NP_003364.1:p.Leu270=
|
|
NM_014000.3:c.809T=
MANE Select
|
NP_054706.1:p.Leu270=
|
|