ENST00000379644.9:c.1566G=
MANE Select
|
ENSP00000368965.4:p.Thr522=
|
|
ENST00000379644.8:c.1566G=
|
ENSP00000368965.4:p.Thr522=
|
|
ENST00000519705.1:n.882G=
|
|
|
ENST00000521576.1:c.717G=
|
ENSP00000429029.1:p.Thr239=
|
|
ENST00000523989.1:n.1879G=
|
|
|
NM_152419.2:c.1566G=
|
NP_689632.2:p.Thr522=
|
|
XM_005273409.1:c.1677G=
|
XP_005273466.1:p.Thr559=
|
|
XM_005273410.1:c.1653G=
|
XP_005273467.1:p.Thr551=
|
|
XM_005273411.1:c.1485G=
|
XP_005273468.1:p.Thr495=
|
|
NM_001363227.1:c.1653G=
|
NP_001350156.1:p.Thr551=
|
|
NM_001363228.1:c.1374G=
|
NP_001350157.1:p.Thr458=
|
|
NM_001363229.1:c.702G=
|
NP_001350158.1:p.Thr234=
|
|
NM_152419.3:c.1566G=
MANE Select
|
NP_689632.2:p.Thr522=
|
|
NM_001363227.2:c.1653G=
|
NP_001350156.1:p.Thr551=
|
|
NM_001363228.2:c.1374G=
|
NP_001350157.1:p.Thr458=
|
|
NM_001363229.2:c.702G=
|
NP_001350158.1:p.Thr234=
|
|