ENST00000304611.13:c.1331A>C
MANE Select
|
ENSP00000303511.8:p.Glu444Ala
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ENST00000244546.4:c.1331A>C
|
ENSP00000244546.4:p.Glu444Ala
|
|
ENST00000304611.12:c.1331A>C
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ENSP00000303511.8:p.Glu444Ala
|
|
NM_000287.3:c.1331A>C
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NP_000278.3:p.Glu444Ala
|
|
NM_001316313.1:c.1067A>C
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NP_001303242.1:p.Glu356Ala
|
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NR_133009.1:n.1424A>C
|
|
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XM_011514661.1:c.1247A>C
|
XP_011512963.1:p.Glu416Ala
|
|
XR_926246.1:n.1424A>C
|
|
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XM_011514661.2:c.1247A>C
|
XP_011512963.1:p.Glu416Ala
|
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XR_001743466.2:n.2405A>C
|
|
|
NM_000287.4:c.1331A>C
MANE Select
|
NP_000278.3:p.Glu444Ala
|
|
NM_001316313.2:c.1067A>C
|
NP_001303242.1:p.Glu356Ala
|
|
NR_133009.2:n.1362A>C
|
|
|