|
NM_000088.4:c.2029-1G>T
MANE Select
|
NP_000079.2:n.2029-1G>T
|
|
ENST00000225964.10:c.2029-1G>T
MANE Select
|
ENSP00000225964.6:n.2029-1G>T
|
|
NM_000088.3:c.2029-1G>T , LRG_1t1:c.2029-1G>T
|
NP_000079.2:n.2029-1G>T
|
|
ENST00000225964.9:c.2029-1G>T
|
ENSP00000225964.5:n.2029-1G>T
|
|
ENST00000476387.1:n.378-1G>T
|
|
|
ENST00000504289.1:n.461-1G>T
|
|
|
XM_005257058.3:c.2029-1G>T
|
XP_005257115.2:n.2029-1G>T
|
|
XM_005257058.4:c.2029-1G>T
|
XP_005257115.2:n.2029-1G>T
|
|
XM_005257059.3:c.1111-1G>T
|
XP_005257116.2:n.1111-1G>T
|
|
XM_005257059.4:c.1111-1G>T
|
XP_005257116.2:n.1111-1G>T
|
|
XM_011524341.1:c.1831-1G>T
|
XP_011522643.1:n.1831-1G>T
|