ENST00000225964.10:c.1669-11C>T
MANE Select
|
ENSP00000225964.6:n.1669-11C>T
|
|
ENST00000225964.9:c.1669-11C>T
|
ENSP00000225964.5:n.1669-11C>T
|
|
ENST00000463440.1:n.59-11C>T
|
|
|
ENST00000471344.1:n.690C>T
|
|
|
ENST00000476387.1:n.7C>T
|
|
|
NM_000088.3:c.1669-11C>T , LRG_1t1:c.1669-11C>T
|
NP_000079.2:n.1669-11C>T
|
|
XM_005257058.3:c.1669-11C>T
|
XP_005257115.2:n.1669-11C>T
|
|
XM_005257059.3:c.958-1359C>T
|
XP_005257116.2:n.958-1359C>T
|
|
XM_011524341.1:c.1471-11C>T
|
XP_011522643.1:n.1471-11C>T
|
|
XM_005257058.4:c.1669-11C>T
|
XP_005257115.2:n.1669-11C>T
|
|
XM_005257059.4:c.958-1359C>T
|
XP_005257116.2:n.958-1359C>T
|
|
NM_000088.4:c.1669-11C>T
MANE Select
|
NP_000079.2:n.1669-11C>T
|
|