NM_004239.4:c.477C>T
MANE Select
|
NP_004230.2:p.Asp159=
|
ENST00000267622.8:c.477C>T
MANE Select
|
ENSP00000267622.4:p.Asp159=
|
NM_001321851.1:c.474C>T
|
NP_001308780.1:p.Asp158=
|
NM_004239.3:c.477C>T
|
NP_004230.2:p.Asp159=
|
ENST00000555516.6:c.-7C>T
|
ENSP00000451944.1:n.-7C>T
|
XM_005268215.2:c.477C>T
|
XP_005268272.1:p.Asp159=
|
XM_006720321.2:c.474C>T
|
XP_006720384.1:p.Asp158=
|
XM_011537361.1:c.477C>T
|
XP_011535663.1:p.Asp159=
|
XM_017021787.2:c.-270C>T
|
XP_016877276.1:n.-270C>T
|
XM_017021788.2:c.-722C>T
|
XP_016877277.1:n.-722C>T
|
XR_001750598.2:n.926C>T
|
|
XR_943560.1:n.932C>T
|
|
XR_943560.2:n.926C>T
|
|