ENST00000400521.7:c.853A>T
MANE Select
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ENSP00000383365.1:p.Arg285Trp
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|
ENST00000334363.14:c.853A>T
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ENSP00000334451.9:p.Arg285Trp
|
|
ENST00000400518.5:c.763A>T
|
ENSP00000383362.1:p.Arg255Trp
|
|
ENST00000400519.6:c.850A>T
|
ENSP00000383363.1:p.Arg284Trp
|
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ENST00000400521.6:c.853A>T
|
ENSP00000383365.1:p.Arg285Trp
|
|
ENST00000400525.6:c.784A>T
|
ENSP00000383369.3:p.Arg262Trp
|
|
ENST00000474308.5:c.796A>T
|
ENSP00000485665.1:p.Arg266Trp
|
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ENST00000475995.3:c.350A>T
|
|
|
ENST00000491939.6:c.757A>T
|
ENSP00000485543.1:p.Arg253Trp
|
|
ENST00000494454.5:n.927A>T
|
|
|
ENST00000542719.6:c.565A>T
|
ENSP00000485128.2:p.Arg189Trp
|
|
ENST00000634537.1:c.82A>T
|
ENSP00000489208.1:p.Arg28Trp
|
|
ENST00000635155.1:n.439A>T
|
|
|
NM_001282512.1:c.853A>T
|
NP_001269441.1:p.Arg285Trp
|
|
NM_006440.4:c.853A>T
|
NP_006431.2:p.Arg285Trp
|
|
NM_001282512.2:c.853A>T
|
NP_001269441.1:p.Arg285Trp
|
|
NM_001352300.1:c.850A>T
|
NP_001339229.1:p.Arg284Trp
|
|
NM_001352301.1:c.763A>T
|
NP_001339230.1:p.Arg255Trp
|
|
NM_001352302.1:c.565A>T
|
NP_001339231.1:p.Arg189Trp
|
|
NM_001352303.1:c.757A>T
|
NP_001339232.1:p.Arg253Trp
|
|
NR_147957.1:n.985A>T
|
|
|
NM_006440.5:c.853A>T
MANE Select
|
NP_006431.2:p.Arg285Trp
|
|
NM_001282512.3:c.853A>T
|
NP_001269441.1:p.Arg285Trp
|
|
NM_001352300.2:c.850A>T
|
NP_001339229.1:p.Arg284Trp
|
|
NR_147957.2:n.811A>T
|
|
|
NM_001352301.2:c.763A>T
|
NP_001339230.1:p.Arg255Trp
|
|
NM_001352302.2:c.565A>T
|
NP_001339231.1:p.Arg189Trp
|
|
NM_001352303.2:c.757A>T
|
NP_001339232.1:p.Arg253Trp
|
|