ENST00000378747.8:c.1148+112T>A
MANE Select
|
ENSP00000368021.3:n.1148+112T>A
|
|
ENST00000263036.9:c.1148+112T>A
|
ENSP00000263036.3:n.1148+112T>A
|
|
ENST00000378747.7:c.1148+112T>A
|
ENSP00000368021.3:n.1148+112T>A
|
|
ENST00000378748.7:c.1148+112T>A
|
ENSP00000368022.3:n.1148+112T>A
|
|
ENST00000378752.7:c.1130+112T>A
|
ENSP00000368027.3:n.1130+112T>A
|
|
ENST00000378757.6:c.1148+112T>A
|
ENSP00000368032.2:n.1148+112T>A
|
|
ENST00000378764.6:c.1130+112T>A
|
ENSP00000368040.1:n.1130+112T>A
|
|
NM_001008211.1:c.1148+112T>A
|
NP_001008212.1:n.1148+112T>A
|
|
NM_001008212.1:c.1148+112T>A
|
NP_001008213.1:n.1148+112T>A
|
|
NM_001008213.1:c.1148+112T>A
|
NP_001008214.1:n.1148+112T>A
|
|
NM_021980.4:c.1148+112T>A
|
NP_068815.2:n.1148+112T>A
|
|
XM_005252336.2:c.1130+112T>A
|
XP_005252393.2:n.1130+112T>A
|
|
XM_005252337.3:c.1130+112T>A
|
XP_005252394.2:n.1130+112T>A
|
|
XM_005252338.2:c.977+112T>A
|
XP_005252395.2:n.977+112T>A
|
|
NM_001008212.2:c.1148+112T>A
MANE Select
|
NP_001008213.1:n.1148+112T>A
|
|