ENST00000383788.10:c.659A>T
MANE Select
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ENSP00000373298.3:p.Glu220Val
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ENST00000604401.2:n.655A>T
|
|
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ENST00000679838.1:c.*421A>T
|
ENSP00000505708.1:n.*421A>T
|
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ENST00000680545.1:n.425A>T
|
|
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ENST00000681097.1:c.659A>T
|
ENSP00000505397.1:p.Glu220Val
|
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ENST00000383781.8:c.629A>T
|
ENSP00000373291.3:p.Glu210Val
|
|
ENST00000383786.9:c.557A>T
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ENSP00000373296.3:p.Glu186Val
|
|
ENST00000383788.9:c.659A>T
|
ENSP00000373298.3:p.Glu220Val
|
|
ENST00000603808.5:c.659A>T
|
ENSP00000474271.1:p.Glu220Val
|
|
ENST00000605797.1:c.488A>T
|
ENSP00000474936.1:p.Glu163Val
|
|
NM_005677.3:c.659A>T
|
NP_005668.2:p.Glu220Val
|
|
NM_080538.2:c.629A>T
|
NP_536799.1:p.Glu210Val
|
|
NM_080539.3:c.557A>T
|
NP_536800.2:p.Glu186Val
|
|
NM_005677.4:c.659A>T
MANE Select
|
NP_005668.2:p.Glu220Val
|
|
NM_080539.4:c.557A>T
|
NP_536800.2:p.Glu186Val
|
|