ENST00000367996.6:c.1262-3C>A
MANE Select
|
ENSP00000356975.4:n.1262-3C>A
|
|
ENST00000367996.5:c.1262-3C>A
|
ENSP00000356975.4:n.1262-3C>A
|
|
ENST00000478394.1:n.288-3C>A
|
|
|
NM_005099.4:c.1262-3C>A
|
NP_005090.3:n.1262-3C>A
|
|
XM_006711635.1:c.1262-3C>A
|
XP_006711698.1:n.1262-3C>A
|
|
NM_001320336.1:c.1262-3C>A
|
NP_001307265.1:n.1262-3C>A
|
|
NM_005099.5:c.1262-3C>A
|
NP_005090.3:n.1262-3C>A
|
|
XR_001737548.2:n.4974-3C>A
|
|
|
XR_001737549.2:n.4974-3C>A
|
|
|
NM_005099.6:c.1262-3C>A
MANE Select
|
NP_005090.3:n.1262-3C>A
|
|
NM_001320336.2:c.1262-3C>A
|
NP_001307265.1:n.1262-3C>A
|
|
NM_001320336.3:c.1262-3C>A
|
NP_001307265.1:n.1262-3C>A
|
|