ENST00000288840.10:c.953-151G>T
MANE Select
|
ENSP00000288840.5:n.953-151G>T
|
|
ENST00000288840.9:c.953-151G>T
|
ENSP00000288840.5:n.953-151G>T
|
|
ENST00000557916.5:c.1085-151G>T
|
ENSP00000452955.1:n.1085-151G>T
|
|
ENST00000559931.5:c.257-151G>T
|
ENSP00000453446.1:n.257-151G>T
|
|
NM_005585.4:c.953-151G>T
|
NP_005576.3:n.953-151G>T
|
|
NR_027654.1:n.2008-151G>T
|
|
|
XM_011521561.1:c.170-151G>T
|
XP_011519863.1:n.170-151G>T
|
|
XR_931825.1:n.2352-151G>T
|
|
|
XM_011521561.2:c.170-151G>T
|
XP_011519863.1:n.170-151G>T
|
|
NM_005585.5:c.953-151G>T
MANE Select
|
NP_005576.3:n.953-151G>T
|
|
NR_027654.2:n.2108-151G>T
|
|
|