|
NM_000088.4:c.3532-3C>T
MANE Select
|
NP_000079.2:n.3532-3C>T
|
|
ENST00000225964.10:c.3532-3C>T
MANE Select
|
ENSP00000225964.6:n.3532-3C>T
|
|
NM_000088.3:c.3532-3C>T , LRG_1t1:c.3532-3C>T
|
NP_000079.2:n.3532-3C>T
|
|
ENST00000225964.9:c.3532-3C>T
|
ENSP00000225964.5:n.3532-3C>T
|
|
ENST00000510710.3:n.198C>T
|
|
|
XM_005257058.3:c.3262-3C>T
|
XP_005257115.2:n.3262-3C>T
|
|
XM_005257058.4:c.3262-3C>T
|
XP_005257115.2:n.3262-3C>T
|
|
XM_005257059.3:c.2614-3C>T
|
XP_005257116.2:n.2614-3C>T
|
|
XM_005257059.4:c.2614-3C>T
|
XP_005257116.2:n.2614-3C>T
|
|
XM_011524341.1:c.3334-3C>T
|
XP_011522643.1:n.3334-3C>T
|