ENST00000371270.6:c.443A>T
MANE Select
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ENSP00000360317.3:p.Glu148Val
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ENST00000371270.5:c.443A>T
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ENSP00000360317.3:p.Glu148Val
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ENST00000479946.2:n.747A>T
|
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ENST00000490994.6:c.*229A>T
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ENSP00000433314.1:n.*229A>T
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ENST00000525991.5:c.*18A>T
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ENSP00000433842.1:n.*18A>T
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ENST00000526814.5:n.698A>T
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|
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ENST00000527420.5:c.443A>T
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ENSP00000433191.1:p.Glu148Val
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ENST00000527953.5:n.698A>T
|
|
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ENST00000533320.5:n.677A>T
|
|
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ENST00000535898.5:c.137A>T
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ENSP00000445062.1:p.Glu46Val
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ENST00000539050.5:c.233A>T
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ENSP00000442343.2:p.Glu78Val
|
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ENST00000623108.3:c.233A>T
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ENSP00000485110.1:p.Glu78Val
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ENST00000628935.1:c.185A>T
|
ENSP00000487145.1:p.Glu62Val
|
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NM_000770.3:c.443A>T
MANE Select
|
NP_000761.3:p.Glu148Val
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NM_001198853.1:c.233A>T
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NP_001185782.1:p.Glu78Val
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NM_001198854.1:c.137A>T
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NP_001185783.1:p.Glu46Val
|
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NM_001198855.1:c.233A>T
|
NP_001185784.1:p.Glu78Val
|
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XR_945610.1:n.539A>T
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