ENST00000298171.7:c.693-11643C>T
MANE Select
|
ENSP00000298171.2:n.693-11643C>T
|
|
ENST00000636454.1:n.611-11643C>T
|
|
|
ENST00000298171.6:c.693-11643C>T
|
ENSP00000298171.2:n.693-11643C>T
|
|
ENST00000541158.6:c.693-11643C>T
|
ENSP00000441235.2:n.693-11643C>T
|
|
NM_000369.2:c.693-11643C>T , LRG_523t1:c.693-11643C>T
|
NP_000360.2:n.693-11643C>T
|
|
XM_005268037.3:c.693-11643C>T
|
XP_005268094.1:n.693-11643C>T
|
|
XM_011537119.1:c.414-11643C>T
|
XP_011535421.1:n.414-11643C>T
|
|
XR_245790.3:n.2087-28510G>A
|
|
|
XR_429385.2:n.854-20856G>A
|
|
|
XR_429386.2:n.855-20898G>A
|
|
|
XR_944075.1:n.866-28510G>A
|
|
|
XR_944076.1:n.862-28510G>A
|
|
|
XR_944077.1:n.866-28510G>A
|
|
|
XR_944078.1:n.866-28510G>A
|
|
|
XR_944079.1:n.856-20856G>A
|
|
|
XM_005268037.4:c.693-11643C>T
|
XP_005268094.1:n.693-11643C>T
|
|
XM_011537119.2:c.414-11643C>T
|
XP_011535421.1:n.414-11643C>T
|
|
XR_001751021.1:n.2754-28510G>A
|
|
|
XR_001751022.1:n.2754-28510G>A
|
|
|
XR_001751023.1:n.2754-28510G>A
|
|
|
XR_944075.3:n.930-28510G>A
|
|
|
NM_000369.4:c.693-11643C>T
|
NP_000360.2:n.693-11643C>T
|
|
NM_000369.5:c.693-11643C>T
MANE Select
|
NP_000360.2:n.693-11643C>T
|
|