ENST00000272895.12:c.4697A>C
MANE Select
|
ENSP00000272895.7:p.Glu1566Ala
|
|
ENST00000272895.11:c.4697A>C
|
ENSP00000272895.7:p.Glu1566Ala
|
|
ENST00000389661.4:c.3743A>C
|
ENSP00000374312.4:p.Glu1248Ala
|
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NM_015657.3:c.3743A>C
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NP_056472.2:p.Glu1248Ala
|
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NM_173076.2:c.4697A>C
|
NP_775099.2:p.Glu1566Ala
|
|
NR_103740.1:n.4997A>C
|
|
|
XM_011510951.1:c.4706A>C
|
XP_011509253.1:p.Glu1569Ala
|
|
XM_011510952.1:c.4706A>C
|
XP_011509254.1:p.Glu1569Ala
|
|
XM_011510951.2:c.4706A>C
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XP_011509253.1:p.Glu1569Ala
|
|
NM_173076.3:c.4697A>C
MANE Select
|
NP_775099.2:p.Glu1566Ala
|
|
NR_103740.2:n.5195A>C
|
|
|
NM_015657.4:c.3743A>C
|
NP_056472.2:p.Glu1248Ala
|
|