ENST00000299314.12:c.-136G>A
MANE Select
|
ENSP00000299314.7:n.-136G>A
|
|
ENST00000299314.11:c.-136G>A
|
ENSP00000299314.7:n.-136G>A
|
|
ENST00000392919.4:c.-136G>A
|
ENSP00000376651.4:n.-136G>A
|
|
ENST00000549940.5:c.-136G>A
|
ENSP00000449150.1:n.-136G>A
|
|
NM_024312.4:c.-136G>A
|
NP_077288.2:n.-136G>A
|
|
XM_006719593.2:c.-136G>A
|
XP_006719656.1:n.-136G>A
|
|
XM_006719593.3:c.-136G>A
|
XP_006719656.1:n.-136G>A
|
|
XM_017019961.1:c.-285G>A
|
XP_016875450.1:n.-285G>A
|
|
XM_017019962.2:c.-1486G>A
|
XP_016875451.1:n.-1486G>A
|
|
NM_024312.5:c.-136G>A
MANE Select
|
NP_077288.2:n.-136G>A
|
|