|
NM_015141.4:c.-51T>C
MANE Select
|
NP_055956.1:n.-51T>C
|
|
ENST00000282541.10:c.-51T>C
MANE Select
|
ENSP00000282541.6:n.-51T>C
|
|
NM_015141.3:c.-51T>C , LRG_419t1:c.-51T>C
|
NP_055956.1:n.-51T>C
|
|
ENST00000282541.9:c.-51T>C
|
ENSP00000282541.5:n.-51T>C
|
|
ENST00000425459.5:c.-51T>C
|
ENSP00000408770.1:n.-51T>C
|
|
ENST00000428684.1:c.-51T>C
|
ENSP00000392199.1:n.-51T>C
|
|
ENST00000429432.5:c.-71+832T>C
|
ENSP00000393861.1:n.-71+832T>C
|
|
XM_005264983.2:c.-51T>C
|
XP_005265040.1:n.-51T>C
|
|
XM_006713068.2:c.-51T>C
|
XP_006713131.1:n.-51T>C
|