NM_181882.3:c.4077_4079dup
MANE Select
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NP_870998.2:p.Glu1360_Glu1361insGlu
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ENST00000324001.8:c.4077_4079dup
MANE Select
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ENSP00000326018.6:p.Glu1360_Glu1361insGlu
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NM_020956.2:c.*4282_*4284dup , LRG_265t1:c.*4282_*4284dup
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NP_066007.1:n.*4282_*4284dup
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NM_181882.2:c.4077_4079dup , LRG_265t2:c.4077_4079dup
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NP_870998.2:p.Glu1360_Glu1361insGlu
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ENST00000291825.11:c.*4282_*4284dup
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ENSP00000291825.6:n.*4282_*4284dup
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ENST00000324001.7:c.4077_4079dup
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ENSP00000326018.6:p.Glu1360_Glu1361insGlu
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ENST00000673881.1:c.3660_3662dup
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ENSP00000501070.1:p.Glu1221_Glu1222insGlu
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ENST00000674005.2:c.4362_4364dup
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ENSP00000501261.1:p.Glu1455_Glu1456insGlu
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ENST00000674773.1:c.3660_3662dup
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ENSP00000502579.1:p.Glu1221_Glu1222insGlu
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ENST00000675517.1:c.3952_3954dup
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ENST00000676076.1:c.3938_3940dup
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ENST00000676260.1:c.4039_4041dup
|
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ENST00000676316.1:c.3964_3966dup
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XM_011527171.1:c.4077_4079dup
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XP_011525473.1:p.Glu1360_Glu1361insGlu
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XM_011527171.2:c.4077_4079dup
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XP_011525473.1:p.Glu1360_Glu1361insGlu
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XM_017027046.1:c.3975_3977dup
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XP_016882535.1:p.Glu1326_Glu1327insGlu
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XM_017027047.1:c.3975_3977dup
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XP_016882536.1:p.Glu1326_Glu1327insGlu
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