ENST00000347454.9:c.739G>T
MANE Select
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ENSP00000233552.6:p.Glu247Ter
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ENST00000347454.8:c.739G>T
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ENSP00000233552.5:p.Glu247Ter
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ENST00000405940.6:c.*5G>T
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ENSP00000384375.2:n.*5G>T
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ENST00000417567.1:c.315G>T
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|
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ENST00000445933.6:c.736G>T
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ENSP00000394397.2:p.Glu246Ter
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ENST00000451130.6:c.799G>T
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ENSP00000394869.2:p.Glu267Ter
|
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ENST00000475582.5:n.2062G>T
|
|
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ENST00000493344.6:c.802G>T
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ENSP00000429323.1:p.Glu268Ter
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ENST00000616081.4:c.730G>T
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ENSP00000477710.1:p.Glu244Ter
|
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ENST00000622434.4:c.*5G>T
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ENSP00000479991.1:n.*5G>T
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|
NM_001034116.1:c.739G>T
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NP_001029288.1:p.Glu247Ter
|
|
NM_015636.3:c.736G>T
|
NP_056451.3:p.Glu246Ter
|
|
NM_172195.3:c.799G>T
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NP_751945.2:p.Glu267Ter
|
|
XM_005264632.1:c.694G>T
|
XP_005264689.1:p.Glu232Ter
|
|
XM_006712132.1:c.691G>T
|
XP_006712195.1:p.Glu231Ter
|
|
XM_011533147.1:c.121G>T
|
XP_011531449.1:p.Glu41Ter
|
|
NM_001318965.1:c.802G>T
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NP_001305894.1:p.Glu268Ter
|
|
NM_001318966.1:c.694G>T
|
NP_001305895.1:p.Glu232Ter
|
|
NM_001318967.1:c.646G>T
|
NP_001305896.1:p.Glu216Ter
|
|
NM_001318968.1:c.154G>T
|
NP_001305897.1:p.Glu52Ter
|
|
NM_001318969.1:c.121G>T
|
NP_001305898.1:p.Glu41Ter
|
|
XM_011533147.2:c.121G>T
|
XP_011531449.1:p.Glu41Ter
|
|
NM_001034116.2:c.739G>T
MANE Select
|
NP_001029288.1:p.Glu247Ter
|
|
NM_001318965.2:c.802G>T
|
NP_001305894.1:p.Glu268Ter
|
|
NM_001318966.2:c.694G>T
|
NP_001305895.1:p.Glu232Ter
|
|
NM_001318967.2:c.646G>T
|
NP_001305896.1:p.Glu216Ter
|
|
NM_001318968.2:c.154G>T
|
NP_001305897.1:p.Glu52Ter
|
|
NM_001318969.2:c.121G>T
|
NP_001305898.1:p.Glu41Ter
|
|
NM_015636.4:c.736G>T
|
NP_056451.3:p.Glu246Ter
|
|
NM_172195.4:c.799G>T
|
NP_751945.2:p.Glu267Ter
|
|