ENST00000264499.9:c.646C>T
MANE Select
|
ENSP00000264499.4:p.Leu216Phe
|
|
ENST00000264499.8:c.646C>T
|
ENSP00000264499.4:p.Leu216Phe
|
|
ENST00000506636.1:c.646C>T
|
ENSP00000423626.1:p.Leu216Phe
|
|
NM_018190.3:c.646C>T
|
NP_060660.2:p.Leu216Phe
|
|
NM_176824.2:c.646C>T
|
NP_789794.1:p.Leu216Phe
|
|
XM_005263106.2:c.649C>T
|
XP_005263163.1:p.Leu217Phe
|
|
XM_011532079.1:c.694C>T
|
XP_011530381.1:p.Leu232Phe
|
|
XM_011532080.1:c.691C>T
|
XP_011530382.1:p.Leu231Phe
|
|
XM_011532081.1:c.694C>T
|
XP_011530383.1:p.Leu232Phe
|
|
XM_005263106.4:c.649C>T
|
XP_005263163.1:p.Leu217Phe
|
|
XM_011532079.3:c.694C>T
|
XP_011530381.1:p.Leu232Phe
|
|
XM_011532080.3:c.691C>T
|
XP_011530382.1:p.Leu231Phe
|
|
XM_011532081.3:c.694C>T
|
XP_011530383.1:p.Leu232Phe
|
|
XM_017008357.2:c.646C>T
|
XP_016863846.1:p.Leu216Phe
|
|
XM_017008358.2:c.649C>T
|
XP_016863847.1:p.Leu217Phe
|
|
NM_176824.3:c.646C>T
MANE Select
|
NP_789794.1:p.Leu216Phe
|
|
NM_018190.4:c.646C>T
|
NP_060660.2:p.Leu216Phe
|
|