ENST00000299314.12:c.934-137A>T
MANE Select
|
ENSP00000299314.7:n.934-137A>T
|
|
ENST00000299314.11:c.934-137A>T
|
ENSP00000299314.7:n.934-137A>T
|
|
ENST00000549940.5:c.934-137A>T
|
ENSP00000449150.1:n.934-137A>T
|
|
NM_024312.4:c.934-137A>T
|
NP_077288.2:n.934-137A>T
|
|
XM_006719593.2:c.934-137A>T
|
XP_006719656.1:n.934-137A>T
|
|
XM_011538731.1:c.853-137A>T
|
XP_011537033.1:n.853-137A>T
|
|
XM_006719593.3:c.934-137A>T
|
XP_006719656.1:n.934-137A>T
|
|
XM_011538731.2:c.853-137A>T
|
XP_011537033.1:n.853-137A>T
|
|
XM_017019961.1:c.718-137A>T
|
XP_016875450.1:n.718-137A>T
|
|
XM_017019962.2:c.-417-14A>T
|
XP_016875451.1:n.-417-14A>T
|
|
NM_024312.5:c.934-137A>T
MANE Select
|
NP_077288.2:n.934-137A>T
|
|