ENST00000316549.11:c.534-13820C>T
MANE Select
|
ENSP00000320246.6:n.534-13820C>T
|
|
ENST00000316549.10:c.534-13820C>T
|
ENSP00000320246.6:n.534-13820C>T
|
|
ENST00000474727.2:c.*145-13820C>T
|
ENSP00000419090.2:n.*145-13820C>T
|
|
NM_173653.3:c.534-13820C>T
|
NP_775924.1:n.534-13820C>T
|
|
XM_011512704.1:c.534-13820C>T
|
XP_011511006.1:n.534-13820C>T
|
|
XM_011512704.3:c.534-13820C>T
|
XP_011511006.1:n.534-13820C>T
|
|
XM_017006202.2:c.534-13820C>T
|
XP_016861691.1:n.534-13820C>T
|
|
XM_017006203.1:c.183-13820C>T
|
XP_016861692.1:n.183-13820C>T
|
|
NM_173653.4:c.534-13820C>T
MANE Select
|
NP_775924.1:n.534-13820C>T
|
|