ENST00000400521.7:c.856A>T
MANE Select
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ENSP00000383365.1:p.Arg286Trp
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ENST00000334363.14:c.856A>T
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ENSP00000334451.9:p.Arg286Trp
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|
ENST00000400518.5:c.766A>T
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ENSP00000383362.1:p.Arg256Trp
|
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ENST00000400519.6:c.853A>T
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ENSP00000383363.1:p.Arg285Trp
|
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ENST00000400521.6:c.856A>T
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ENSP00000383365.1:p.Arg286Trp
|
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ENST00000400525.6:c.787A>T
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ENSP00000383369.3:p.Arg263Trp
|
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ENST00000474308.5:c.799A>T
|
ENSP00000485665.1:p.Arg267Trp
|
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ENST00000475995.3:c.353A>T
|
|
|
ENST00000491939.6:c.760A>T
|
ENSP00000485543.1:p.Arg254Trp
|
|
ENST00000494454.5:n.930A>T
|
|
|
ENST00000542719.6:c.568A>T
|
ENSP00000485128.2:p.Arg190Trp
|
|
ENST00000634537.1:c.85A>T
|
ENSP00000489208.1:p.Arg29Trp
|
|
ENST00000635155.1:n.442A>T
|
|
|
NM_001282512.1:c.856A>T
|
NP_001269441.1:p.Arg286Trp
|
|
NM_006440.4:c.856A>T
|
NP_006431.2:p.Arg286Trp
|
|
NM_001282512.2:c.856A>T
|
NP_001269441.1:p.Arg286Trp
|
|
NM_001352300.1:c.853A>T
|
NP_001339229.1:p.Arg285Trp
|
|
NM_001352301.1:c.766A>T
|
NP_001339230.1:p.Arg256Trp
|
|
NM_001352302.1:c.568A>T
|
NP_001339231.1:p.Arg190Trp
|
|
NM_001352303.1:c.760A>T
|
NP_001339232.1:p.Arg254Trp
|
|
NR_147957.1:n.988A>T
|
|
|
NM_006440.5:c.856A>T
MANE Select
|
NP_006431.2:p.Arg286Trp
|
|
NM_001282512.3:c.856A>T
|
NP_001269441.1:p.Arg286Trp
|
|
NM_001352300.2:c.853A>T
|
NP_001339229.1:p.Arg285Trp
|
|
NR_147957.2:n.814A>T
|
|
|
NM_001352301.2:c.766A>T
|
NP_001339230.1:p.Arg256Trp
|
|
NM_001352302.2:c.568A>T
|
NP_001339231.1:p.Arg190Trp
|
|
NM_001352303.2:c.760A>T
|
NP_001339232.1:p.Arg254Trp
|
|