ENST00000072644.7:c.*9-2394T>C
MANE Select
|
ENSP00000072644.1:n.*9-2394T>C
|
|
ENST00000072644.5:c.*9-2394T>C
|
ENSP00000072644.1:n.*9-2394T>C
|
|
ENST00000371399.5:c.*9-2394T>C
|
ENSP00000360452.1:n.*9-2394T>C
|
|
ENST00000464950.6:c.*59+337T>C
|
ENSP00000432266.1:n.*59+337T>C
|
|
NM_018982.4:c.*9-2394T>C
|
NP_061855.1:n.*9-2394T>C
|
|
NR_036639.1:n.1351+337T>C
|
|
|
NR_036640.1:n.1131+337T>C
|
|
|
XM_011541600.1:c.*9-4852T>C
|
XP_011539902.1:n.*9-4852T>C
|
|
XM_011541601.1:c.*59+337T>C
|
XP_011539903.1:n.*59+337T>C
|
|
XM_011541602.1:c.*59+337T>C
|
XP_011539904.1:n.*59+337T>C
|
|
XM_011541603.1:c.*59+337T>C
|
XP_011539905.1:n.*59+337T>C
|
|
XM_011541604.1:c.*9-2394T>C
|
XP_011539906.1:n.*9-2394T>C
|
|
XM_011541605.1:c.*59+337T>C
|
XP_011539907.1:n.*59+337T>C
|
|
NR_135075.1:n.1018-2394T>C
|
|
|
XM_017001499.2:c.*9-2394T>C
|
XP_016856988.1:n.*9-2394T>C
|
|
XM_017001500.1:c.*9-2394T>C
|
XP_016856989.1:n.*9-2394T>C
|
|
XM_017001501.1:c.*9-2394T>C
|
XP_016856990.1:n.*9-2394T>C
|
|
XR_001737231.1:n.1172+337T>C
|
|
|
XR_001737232.1:n.957+337T>C
|
|
|
XR_001737233.1:n.1053+337T>C
|
|
|
XR_001737234.1:n.873+337T>C
|
|
|
NM_018982.5:c.*9-2394T>C
MANE Select
|
NP_061855.1:n.*9-2394T>C
|
|
NR_036639.2:n.1334+337T>C
|
|
|
NR_036640.2:n.1114+337T>C
|
|
|
NR_135075.2:n.984-2394T>C
|
|
|