ENST00000302347.10:c.1111G>T
|
ENSP00000303242.6:p.Glu371Ter
|
|
ENST00000652462.1:c.1039G>T
MANE Select
|
ENSP00000498780.1:p.Glu347Ter
|
|
ENST00000302347.9:c.1039G>T
|
ENSP00000303242.5:p.Glu347Ter
|
|
ENST00000355153.8:c.1039G>T
|
ENSP00000347279.4:p.Glu347Ter
|
|
ENST00000397850.6:c.1039G>T
|
ENSP00000380948.2:p.Glu347Ter
|
|
ENST00000397852.5:c.1039G>T
|
ENSP00000380950.1:p.Glu347Ter
|
|
ENST00000397854.7:c.868G>T
|
ENSP00000380952.3:p.Glu290Ter
|
|
ENST00000397857.5:c.1039G>T
|
ENSP00000380955.1:p.Glu347Ter
|
|
ENST00000498666.5:n.1182G>T
|
|
|
ENST00000523323.5:c.*866G>T
|
ENSP00000427732.1:n.*866G>T
|
|
ENST00000610622.4:c.868G>T
|
ENSP00000480700.1:p.Glu290Ter
|
|
NM_000211.4:c.1039G>T
|
NP_000202.3:p.Glu347Ter
|
|
NM_001127491.2:c.1039G>T
|
NP_001120963.2:p.Glu347Ter
|
|
NM_001303238.1:c.832G>T
|
NP_001290167.1:p.Glu278Ter
|
|
XM_006724001.1:c.832G>T
|
XP_006724064.1:p.Glu278Ter
|
|
XM_006724001.2:c.832G>T
|
XP_006724064.1:p.Glu278Ter
|
|
NM_000211.5:c.1039G>T
MANE Select
|
NP_000202.3:p.Glu347Ter
|
|
NM_001127491.3:c.1039G>T
|
NP_001120963.2:p.Glu347Ter
|
|
NM_001303238.2:c.832G>T
|
NP_001290167.1:p.Glu278Ter
|
|