ENST00000552864.6:c.83-8779C>T
MANE Select
|
ENSP00000447488.1:n.83-8779C>T
|
|
ENST00000261203.7:c.83-8779C>T
|
ENSP00000261203.3:n.83-8779C>T
|
|
ENST00000549417.5:c.65-8779C>T
|
ENSP00000448975.1:n.65-8779C>T
|
|
ENST00000552864.5:c.83-8779C>T
|
ENSP00000447488.1:n.83-8779C>T
|
|
NM_004664.2:c.83-8779C>T
|
NP_004655.1:n.83-8779C>T
|
|
XM_011538928.1:c.83-8779C>T
|
XP_011537230.1:n.83-8779C>T
|
|
NM_001324423.1:c.-13+39493C>T
|
NP_001311352.1:n.-13+39493C>T
|
|
NM_004664.3:c.83-8779C>T
|
NP_004655.1:n.83-8779C>T
|
|
NR_136887.1:n.275+39493C>T
|
|
|
NR_136888.1:n.276-8779C>T
|
|
|
XM_011538928.3:c.44-8779C>T
|
XP_011537230.2:n.44-8779C>T
|
|
NM_001324423.2:c.-13+39493C>T
|
NP_001311352.1:n.-13+39493C>T
|
|
NR_136887.2:n.67+39493C>T
|
|
|
NR_136888.2:n.68-8779C>T
|
|
|
NM_004664.4:c.83-8779C>T
MANE Select
|
NP_004655.1:n.83-8779C>T
|
|
NR_136888.3:n.295-8779C>T
|
|
|