ENST00000682028.1:c.1371A>T
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ENSP00000507230.1:p.Ala457=
|
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ENST00000682268.1:n.1669A>T
|
|
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ENST00000682676.1:n.772A>T
|
|
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ENST00000682902.1:n.1673A>T
|
|
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ENST00000683513.1:c.1371A>T
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ENSP00000506809.1:p.Ala457=
|
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ENST00000263431.4:c.1371A>T
MANE Select
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ENSP00000263431.3:p.Ala457=
|
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ENST00000263431.3:c.1371A>T
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ENSP00000263431.3:p.Ala457=
|
|
NM_001316329.1:c.1371A>T
|
NP_001303258.1:p.Ala457=
|
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NM_002739.3:c.1371A>T , LRG_669t1:c.1371A>T
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NP_002730.1:p.Ala457=
|
|
NM_002739.4:c.1371A>T
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NP_002730.1:p.Ala457=
|
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XM_011527108.1:c.462A>T
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XP_011525410.1:p.Ala154=
|
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NM_002739.5:c.1371A>T
MANE Select
|
NP_002730.1:p.Ala457=
|
|
NM_001316329.2:c.1371A>T
|
NP_001303258.1:p.Ala457=
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