ENST00000336232.7:c.883G>T
MANE Select
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ENSP00000337335.2:p.Glu295Ter
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ENST00000311438.12:c.883G>T
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ENSP00000311463.8:p.Glu295Ter
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ENST00000336232.6:c.883G>T
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ENSP00000337335.2:p.Glu295Ter
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ENST00000430500.6:c.883G>T
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ENSP00000398548.2:p.Glu295Ter
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ENST00000535878.5:c.514G>T
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ENSP00000443368.1:p.Glu172Ter
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ENST00000539841.1:n.701G>T
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|
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ENST00000545207.5:c.610G>T
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ENSP00000441658.1:p.Glu204Ter
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NM_001184732.1:c.883G>T
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NP_001171661.1:p.Glu295Ter
|
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NM_001184733.1:c.610G>T
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NP_001171662.1:p.Glu204Ter
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NM_001184736.1:c.514G>T
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NP_001171665.1:p.Glu172Ter
|
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NM_004254.3:c.883G>T
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NP_004245.2:p.Glu295Ter
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XM_011545364.1:c.514G>T
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XP_011543666.1:p.Glu172Ter
|
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NM_004254.4:c.883G>T
MANE Select
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NP_004245.2:p.Glu295Ter
|
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NM_001184732.2:c.883G>T
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NP_001171661.1:p.Glu295Ter
|
|
NM_001184733.2:c.610G>T
|
NP_001171662.1:p.Glu204Ter
|
|
NM_001184736.2:c.514G>T
|
NP_001171665.1:p.Glu172Ter
|
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