ENST00000302746.11:c.485T>A
MANE Select
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ENSP00000307241.6:p.Phe162Tyr
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ENST00000302746.10:c.485T>A
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ENSP00000307241.6:p.Phe162Tyr
|
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ENST00000383714.8:c.431T>A
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ENSP00000373220.4:p.Phe144Tyr
|
|
ENST00000461692.5:n.598T>A
|
|
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ENST00000469364.5:c.485T>A
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ENSP00000419580.1:p.Phe162Tyr
|
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ENST00000474765.1:c.431T>A
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ENSP00000418448.1:p.Phe144Tyr
|
|
ENST00000479945.1:n.2890T>A
|
|
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ENST00000480626.5:n.577T>A
|
|
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ENST00000485460.5:c.431T>A
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ENSP00000417267.1:p.Phe144Tyr
|
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NM_000925.3:c.485T>A
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NP_000916.2:p.Phe162Tyr
|
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NM_001173468.1:c.431T>A
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NP_001166939.1:p.Phe144Tyr
|
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NM_001315536.1:c.431T>A
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NP_001302465.1:p.Phe144Tyr
|
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NR_033384.1:n.598T>A
|
|
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NM_000925.4:c.485T>A
MANE Select
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NP_000916.2:p.Phe162Tyr
|
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NM_001173468.2:c.431T>A
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NP_001166939.1:p.Phe144Tyr
|
|
NM_001315536.2:c.431T>A
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NP_001302465.1:p.Phe144Tyr
|
|
NR_033384.2:n.591T>A
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|
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