ENST00000347230.9:c.4301A>C
MANE Select
|
ENSP00000251119.5:p.Glu1434Ala
|
|
ENST00000676512.1:c.4301A>C
|
ENSP00000504552.1:p.Glu1434Ala
|
|
ENST00000676620.1:c.4301A>C
|
ENSP00000504587.1:p.Glu1434Ala
|
|
ENST00000678386.1:c.4301A>C
|
ENSP00000503677.1:p.Glu1434Ala
|
|
ENST00000347230.8:c.4301A>C
|
ENSP00000251119.5:p.Glu1434Ala
|
|
ENST00000554523.5:n.4438A>C
|
|
|
ENST00000554557.5:c.*2350+248A>C
|
ENSP00000450431.1:n.*2350+248A>C
|
|
ENST00000555452.1:c.4301A>C
|
ENSP00000450603.1:p.Glu1434Ala
|
|
NM_015346.3:c.4301A>C
|
NP_056161.2:p.Glu1434Ala
|
|
XM_006720093.2:c.4301A>C
|
XP_006720156.1:p.Glu1434Ala
|
|
XM_011536606.1:c.2792A>C
|
XP_011534908.1:p.Glu931Ala
|
|
XM_011536607.1:c.1976A>C
|
XP_011534909.1:p.Glu659Ala
|
|
XM_011536608.1:c.1883A>C
|
XP_011534910.1:p.Glu628Ala
|
|
XM_011536609.1:c.4301A>C
|
XP_011534911.1:p.Glu1434Ala
|
|
XM_011536609.2:c.4301A>C
|
XP_011534911.1:p.Glu1434Ala
|
|
XM_017021124.1:c.4301A>C
|
XP_016876613.1:p.Glu1434Ala
|
|
XM_017021125.1:c.4301A>C
|
XP_016876614.1:p.Glu1434Ala
|
|
XM_017021126.1:c.2792A>C
|
XP_016876615.1:p.Glu931Ala
|
|
XM_017021127.2:c.1976A>C
|
XP_016876616.1:p.Glu659Ala
|
|
XM_017021128.1:c.1883A>C
|
XP_016876617.1:p.Glu628Ala
|
|
NM_015346.4:c.4301A>C
MANE Select
|
NP_056161.2:p.Glu1434Ala
|
|