ENST00000594866.3:c.1251T>A
MANE Select
|
ENSP00000469738.2:p.Pro417=
|
|
ENST00000614245.2:c.525T>A
|
ENSP00000480219.2:p.Pro175=
|
|
ENST00000396720.7:c.1251T>A
|
ENSP00000379946.2:p.Pro417=
|
|
ENST00000614245.1:c.1095T>A
|
ENSP00000480219.1:p.Pro365=
|
|
NM_015711.3:c.1251T>A
|
NP_056526.3:p.Pro417=
|
|
XM_005258833.3:c.1251T>A
|
XP_005258890.1:p.Pro417=
|
|
XM_006723180.2:c.1251T>A
|
XP_006723243.1:p.Pro417=
|
|
XM_011526882.1:c.1113T>A
|
XP_011525184.1:p.Pro371=
|
|
XM_011526883.1:c.1251T>A
|
XP_011525185.1:p.Pro417=
|
|
XM_005258833.4:c.1251T>A
|
XP_005258890.1:p.Pro417=
|
|
XM_006723180.3:c.1251T>A
|
XP_006723243.1:p.Pro417=
|
|
XM_011526882.2:c.1113T>A
|
XP_011525184.1:p.Pro371=
|
|
XM_011526883.2:c.1251T>A
|
XP_011525185.1:p.Pro417=
|
|
NM_001394372.1:c.1251T>A
MANE Select
|
NP_001381301.1:p.Pro417=
|
|