ENST00000700555.2:n.763A=
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|
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ENST00000700557.2:n.352A=
|
|
|
ENST00000700559.2:c.2168-3475A=
|
ENSP00000515065.2:n.2168-3475A=
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|
ENST00000546498.2:n.947A=
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|
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ENST00000549461.2:n.752A=
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ENST00000700555.1:c.691A=
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ENSP00000515062.1:p.Thr231=
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|
ENST00000700556.1:c.731A=
|
|
|
ENST00000700557.1:c.271A=
|
ENSP00000515064.1:p.Thr91=
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|
ENST00000700558.1:n.474A=
|
|
|
ENST00000700559.1:c.1383-3475A=
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|
|
ENST00000700560.1:n.1475A=
|
|
|
ENST00000700561.1:n.1601A=
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|
|
ENST00000070846.11:c.2392A=
|
ENSP00000070846.6:p.Thr798=
|
|
ENST00000340811.9:c.2260A=
MANE Select
|
ENSP00000342800.5:p.Thr754=
|
|
ENST00000070846.10:c.2392A=
|
ENSP00000070846.6:p.Thr798=
|
|
ENST00000340811.8:c.2260A=
|
ENSP00000342800.4:p.Thr754=
|
|
ENST00000613243.1:c.2392A=
|
ENSP00000478295.1:p.Thr798=
|
|
NM_001005242.2:c.2260A=
|
NP_001005242.2:p.Thr754=
|
|
NM_004572.3:c.2392A= , LRG_398t1:c.2392A=
|
NP_004563.2:p.Thr798=
|
|
NM_001005242.3:c.2260A=
MANE Select
|
NP_001005242.2:p.Thr754=
|
|
NM_004572.4:c.2392A=
|
NP_004563.2:p.Thr798=
|
|