|
NM_000088.4:c.3814+2T>C
MANE Select
|
NP_000079.2:n.3814+2T>C
|
|
ENST00000225964.10:c.3814+2T>C
MANE Select
|
ENSP00000225964.6:n.3814+2T>C
|
|
NM_000088.3:c.3814+2T>C , LRG_1t1:c.3814+2T>C
|
NP_000079.2:n.3814+2T>C
|
|
ENST00000225964.9:c.3814+2T>C
|
ENSP00000225964.5:n.3814+2T>C
|
|
ENST00000510710.3:n.483+2T>C
|
|
|
XM_005257058.3:c.3544+2T>C
|
XP_005257115.2:n.3544+2T>C
|
|
XM_005257058.4:c.3544+2T>C
|
XP_005257115.2:n.3544+2T>C
|
|
XM_005257059.3:c.2896+2T>C
|
XP_005257116.2:n.2896+2T>C
|
|
XM_005257059.4:c.2896+2T>C
|
XP_005257116.2:n.2896+2T>C
|
|
XM_011524341.1:c.3616+2T>C
|
XP_011522643.1:n.3616+2T>C
|