ENST00000237596.7:c.1548+161G>T
MANE Select
|
ENSP00000237596.2:n.1548+161G>T
|
|
ENST00000237596.6:c.1548+161G>T
|
ENSP00000237596.2:n.1548+161G>T
|
|
ENST00000508588.5:c.-199+3574G>T
|
ENSP00000427131.1:n.-199+3574G>T
|
|
NM_000297.3:c.1548+161G>T
|
NP_000288.1:n.1548+161G>T
|
|
XM_011532028.1:c.1323+161G>T
|
XP_011530330.1:n.1323+161G>T
|
|
XM_011532029.1:c.828+161G>T
|
XP_011530331.1:n.828+161G>T
|
|
XM_011532030.1:c.708+161G>T
|
XP_011530332.1:n.708+161G>T
|
|
XR_244632.2:n.1643+161G>T
|
|
|
NR_156488.1:n.1635+161G>T
|
|
|
XM_011532028.2:c.1323+161G>T
|
XP_011530330.1:n.1323+161G>T
|
|
XM_011532030.2:c.708+161G>T
|
XP_011530332.1:n.708+161G>T
|
|
NM_000297.4:c.1548+161G>T
MANE Select
|
NP_000288.1:n.1548+161G>T
|
|
NR_156488.2:n.1647+161G>T
|
|
|