ENST00000400521.7:c.887G>A
MANE Select
|
ENSP00000383365.1:p.Trp296Ter
|
|
ENST00000334363.14:c.887G>A
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ENSP00000334451.9:p.Trp296Ter
|
|
ENST00000400518.5:c.797G>A
|
ENSP00000383362.1:p.Trp266Ter
|
|
ENST00000400519.6:c.884G>A
|
ENSP00000383363.1:p.Trp295Ter
|
|
ENST00000400521.6:c.887G>A
|
ENSP00000383365.1:p.Trp296Ter
|
|
ENST00000400525.6:c.818G>A
|
ENSP00000383369.3:p.Trp273Ter
|
|
ENST00000474308.5:c.830G>A
|
ENSP00000485665.1:p.Trp277Ter
|
|
ENST00000475995.3:c.384G>A
|
|
|
ENST00000491939.6:c.791G>A
|
ENSP00000485543.1:p.Trp264Ter
|
|
ENST00000494454.5:n.961G>A
|
|
|
ENST00000542719.6:c.599G>A
|
ENSP00000485128.2:p.Trp200Ter
|
|
ENST00000634537.1:c.116G>A
|
ENSP00000489208.1:p.Trp39Ter
|
|
ENST00000635155.1:n.473G>A
|
|
|
NM_001282512.1:c.887G>A
|
NP_001269441.1:p.Trp296Ter
|
|
NM_006440.4:c.887G>A
|
NP_006431.2:p.Trp296Ter
|
|
NM_001282512.2:c.887G>A
|
NP_001269441.1:p.Trp296Ter
|
|
NM_001352300.1:c.884G>A
|
NP_001339229.1:p.Trp295Ter
|
|
NM_001352301.1:c.797G>A
|
NP_001339230.1:p.Trp266Ter
|
|
NM_001352302.1:c.599G>A
|
NP_001339231.1:p.Trp200Ter
|
|
NM_001352303.1:c.791G>A
|
NP_001339232.1:p.Trp264Ter
|
|
NR_147957.1:n.1019G>A
|
|
|
NM_006440.5:c.887G>A
MANE Select
|
NP_006431.2:p.Trp296Ter
|
|
NM_001282512.3:c.887G>A
|
NP_001269441.1:p.Trp296Ter
|
|
NM_001352300.2:c.884G>A
|
NP_001339229.1:p.Trp295Ter
|
|
NR_147957.2:n.845G>A
|
|
|
NM_001352301.2:c.797G>A
|
NP_001339230.1:p.Trp266Ter
|
|
NM_001352302.2:c.599G>A
|
NP_001339231.1:p.Trp200Ter
|
|
NM_001352303.2:c.791G>A
|
NP_001339232.1:p.Trp264Ter
|
|