ENST00000264499.9:c.1987C>T
MANE Select
|
ENSP00000264499.4:p.Gln663Ter
|
|
ENST00000264499.8:c.1987C>T
|
ENSP00000264499.4:p.Gln663Ter
|
|
ENST00000506636.1:c.1987C>T
|
ENSP00000423626.1:p.Gln663Ter
|
|
ENST00000507814.5:c.256C>T
|
ENSP00000423250.1:p.Gln86Ter
|
|
NM_018190.3:c.1987C>T
|
NP_060660.2:p.Gln663Ter
|
|
NM_176824.2:c.1987C>T
|
NP_789794.1:p.Gln663Ter
|
|
XM_005263106.2:c.1990C>T
|
XP_005263163.1:p.Gln664Ter
|
|
XM_011532079.1:c.2035C>T
|
XP_011530381.1:p.Gln679Ter
|
|
XM_011532080.1:c.2032C>T
|
XP_011530382.1:p.Gln678Ter
|
|
XM_011532081.1:c.1870C>T
|
XP_011530383.1:p.Gln624Ter
|
|
XM_005263106.4:c.1990C>T
|
XP_005263163.1:p.Gln664Ter
|
|
XM_011532079.3:c.2035C>T
|
XP_011530381.1:p.Gln679Ter
|
|
XM_011532080.3:c.2032C>T
|
XP_011530382.1:p.Gln678Ter
|
|
XM_011532081.3:c.1870C>T
|
XP_011530383.1:p.Gln624Ter
|
|
XM_017008357.2:c.1822C>T
|
XP_016863846.1:p.Gln608Ter
|
|
XM_017008358.2:c.1825C>T
|
XP_016863847.1:p.Gln609Ter
|
|
NM_176824.3:c.1987C>T
MANE Select
|
NP_789794.1:p.Gln663Ter
|
|
NM_018190.4:c.1987C>T
|
NP_060660.2:p.Gln663Ter
|
|