ENST00000260408.8:c.420A>C
MANE Select
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ENSP00000260408.3:p.Ala140=
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ENST00000260408.7:c.420A>C
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ENSP00000260408.3:p.Ala140=
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ENST00000396136.6:c.95A>C
|
|
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ENST00000402627.5:c.56-38358A>C
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ENSP00000386056.1:n.56-38358A>C
|
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ENST00000439637.5:c.325+3008A>C
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ENSP00000391930.1:n.325+3008A>C
|
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ENST00000497846.5:n.537A>C
|
|
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ENST00000558004.1:c.332-13991A>C
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ENSP00000452704.1:n.332-13991A>C
|
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ENST00000558733.5:n.656A>C
|
|
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ENST00000559053.1:c.56-38358A>C
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ENSP00000453952.1:n.56-38358A>C
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ENST00000560608.5:n.558A>C
|
|
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ENST00000561288.1:c.55+70292A>C
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ENSP00000452639.1:n.55+70292A>C
|
|
NM_001110.3:c.420A>C
|
NP_001101.1:p.Ala140=
|
|
XM_005254117.2:c.420A>C
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XP_005254174.1:p.Ala140=
|
|
NM_001320570.1:c.420A>C
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NP_001307499.1:p.Ala140=
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XM_024449818.1:c.198A>C
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XP_024305586.1:p.Ala66=
|
|
NM_001110.4:c.420A>C
MANE Select
|
NP_001101.1:p.Ala140=
|
|
NM_001320570.2:c.420A>C
|
NP_001307499.1:p.Ala140=
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