ENST00000594866.3:c.1165C>T
MANE Select
|
ENSP00000469738.2:p.Gln389Ter
|
|
ENST00000614245.2:c.439C>T
|
ENSP00000480219.2:p.Gln147Ter
|
|
ENST00000396720.7:c.1165C>T
|
ENSP00000379946.2:p.Gln389Ter
|
|
ENST00000614245.1:c.1009C>T
|
ENSP00000480219.1:p.Gln337Ter
|
|
NM_015711.3:c.1165C>T
|
NP_056526.3:p.Gln389Ter
|
|
XM_005258833.3:c.1165C>T
|
XP_005258890.1:p.Gln389Ter
|
|
XM_006723180.2:c.1165C>T
|
XP_006723243.1:p.Gln389Ter
|
|
XM_011526882.1:c.1027C>T
|
XP_011525184.1:p.Gln343Ter
|
|
XM_011526883.1:c.1165C>T
|
XP_011525185.1:p.Gln389Ter
|
|
XM_005258833.4:c.1165C>T
|
XP_005258890.1:p.Gln389Ter
|
|
XM_006723180.3:c.1165C>T
|
XP_006723243.1:p.Gln389Ter
|
|
XM_011526882.2:c.1027C>T
|
XP_011525184.1:p.Gln343Ter
|
|
XM_011526883.2:c.1165C>T
|
XP_011525185.1:p.Gln389Ter
|
|
NM_001394372.1:c.1165C>T
MANE Select
|
NP_001381301.1:p.Gln389Ter
|
|