ENST00000262493.12:c.869A>T
MANE Select
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ENSP00000262493.6:p.Glu290Val
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ENST00000562316.6:c.536A>T
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ENSP00000457238.2:p.Glu179Val
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ENST00000564727.2:c.173A>T
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ENSP00000454971.2:p.Glu58Val
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ENST00000568375.2:c.116-3337A>T
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ENST00000638185.1:n.1084A>T
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ENST00000638210.1:n.1169A>T
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|
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ENST00000638705.1:c.869A>T
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ENSP00000491223.1:p.Glu290Val
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ENST00000638836.1:n.779A>T
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ENST00000639055.1:n.1590A>T
|
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ENST00000639251.1:n.770A>T
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ENST00000639268.1:c.504A>T
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ENST00000639341.1:c.394A>T
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|
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ENST00000639770.1:c.907A>T
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ENSP00000491999.1:n.907A>T
|
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ENST00000640390.1:n.799A>T
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|
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ENST00000640469.1:c.233A>T
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ENSP00000491875.1:p.Glu78Val
|
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ENST00000640560.1:n.645A>T
|
|
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ENST00000640893.1:c.*267A>T
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ENSP00000492677.1:n.*267A>T
|
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ENST00000262493.10:c.869A>T
|
ENSP00000262493.6:p.Glu290Val
|
|
ENST00000564727.1:c.89A>T
|
ENSP00000454971.1:p.Glu30Val
|
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ENST00000568375.1:n.116-3337A>T
|
|
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NM_020988.2:c.869A>T
|
NP_066268.1:p.Glu290Val
|
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XM_011523003.1:c.743A>T
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XP_011521305.1:p.Glu248Val
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XM_011523003.3:c.743A>T
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XP_011521305.1:p.Glu248Val
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NM_020988.3:c.869A>T
MANE Select
|
NP_066268.1:p.Glu290Val
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