ENST00000298171.7:c.1013A=
MANE Select
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ENSP00000298171.2:p.Lys338=
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ENST00000636454.1:n.931A=
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|
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ENST00000298171.6:c.1013A=
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ENSP00000298171.2:p.Lys338=
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ENST00000541158.6:c.1013A=
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ENSP00000441235.2:p.Lys338=
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NM_000369.2:c.1013A= , LRG_523t1:c.1013A=
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NP_000360.2:p.Lys338=
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XM_005268037.3:c.1013A=
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XP_005268094.1:p.Lys338=
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XM_011537119.1:c.734A=
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XP_011535421.1:p.Lys245=
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XR_245790.3:n.2086+22122T=
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|
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XR_429385.2:n.853+22122T=
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XR_429386.2:n.854+22122T=
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XR_944075.1:n.865+22122T=
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|
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XR_944076.1:n.861+22122T=
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|
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XR_944077.1:n.865+22122T=
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|
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XR_944078.1:n.865+22122T=
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|
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XR_944079.1:n.855+22122T=
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|
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XM_005268037.4:c.1013A=
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XP_005268094.1:p.Lys338=
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|
XM_011537119.2:c.734A=
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XP_011535421.1:p.Lys245=
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|
XR_001751021.1:n.2753+22122T=
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|
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XR_001751022.1:n.2753+22122T=
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|
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XR_001751023.1:n.2753+22122T=
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|
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XR_944075.3:n.929+22122T=
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|
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NM_000369.4:c.1013A=
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NP_000360.2:p.Lys338=
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|
NM_000369.5:c.1013A=
MANE Select
|
NP_000360.2:p.Lys338=
|
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