ENST00000367615.9:c.534+141A=
MANE Select
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ENSP00000356587.4:n.534+141A=
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ENST00000367615.8:c.534+141A=
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ENSP00000356587.4:n.534+141A=
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ENST00000367616.4:c.534+141A=
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ENSP00000356588.4:n.534+141A=
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NM_001297575.1:c.534+141A=
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NP_001284504.1:n.534+141A=
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NM_014625.3:c.534+141A= , LRG_887t1:c.534+141A=
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NP_055440.1:n.534+141A=
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XM_005245483.2:c.357+141A=
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XP_005245540.1:n.357+141A=
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XM_006711529.2:c.534+141A=
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XP_006711592.1:n.534+141A=
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XM_005245483.3:c.357+141A=
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XP_005245540.1:n.357+141A=
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XM_017002298.1:c.461+141A=
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XP_016857787.1:n.461+141A=
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XM_017002299.1:c.534+141A=
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XP_016857788.1:n.534+141A=
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NM_001297575.2:c.534+141A=
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NP_001284504.1:n.534+141A=
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NM_014625.4:c.534+141A=
MANE Select
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NP_055440.1:n.534+141A=
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