ENST00000622235.5:c.1789G>A
MANE Select
|
ENSP00000477564.2:p.Glu597Lys
|
|
ENST00000494535.1:n.680G>A
|
|
|
ENST00000615031.4:c.1804G>A
|
ENSP00000479389.1:p.Glu602Lys
|
|
ENST00000622235.4:c.1789G>A
|
ENSP00000477564.1:p.Glu597Lys
|
|
ENST00000623402.1:c.1804G>A
|
ENSP00000485276.1:p.Glu602Lys
|
|
NM_153334.6:c.1804G>A
|
NP_699165.3:p.Glu602Lys
|
|
NM_182895.4:c.1789G>A
|
NP_878315.2:p.Glu597Lys
|
|
XM_017029065.2:c.*18G>A
|
XP_016884554.1:n.*18G>A
|
|
NM_153334.7:c.1804G>A
|
NP_699165.3:p.Glu602Lys
|
|
NM_182895.5:c.1789G>A
MANE Select
|
NP_878315.2:p.Glu597Lys
|
|