ENST00000354638.8:c.-21-8663C>T
MANE Select
|
ENSP00000346659.3:n.-21-8663C>T
|
|
ENST00000353809.9:c.-21-8663C>T
|
ENSP00000261276.8:n.-21-8663C>T
|
|
ENST00000354638.7:c.-21-8663C>T
|
ENSP00000346659.3:n.-21-8663C>T
|
|
ENST00000431101.1:c.-22+8553C>T
|
ENSP00000415431.1:n.-22+8553C>T
|
|
ENST00000445578.5:c.-21-8663C>T
|
ENSP00000414425.1:n.-21-8663C>T
|
|
NM_000275.2:c.-21-8663C>T
|
NP_000266.2:n.-21-8663C>T
|
|
NM_001300984.1:c.-21-8663C>T
|
NP_001287913.1:n.-21-8663C>T
|
|
XM_011521640.1:c.-21-8663C>T
|
XP_011519942.1:n.-21-8663C>T
|
|
XM_011521640.2:c.-21-8663C>T
|
XP_011519942.1:n.-21-8663C>T
|
|
NM_000275.3:c.-21-8663C>T
MANE Select
|
NP_000266.2:n.-21-8663C>T
|
|
NM_001300984.2:c.-21-8663C>T
|
NP_001287913.1:n.-21-8663C>T
|
|