ENST00000695651.1:n.2978+133G>T
|
|
|
ENST00000695653.1:c.2539+133G>T
|
ENSP00000512084.1:n.2539+133G>T
|
|
ENST00000695654.1:c.3655+133G>T
|
ENSP00000512085.1:n.3655+133G>T
|
|
ENST00000695689.1:c.601+133G>T
|
ENSP00000512101.1:n.601+133G>T
|
|
ENST00000695690.1:n.1695+133G>T
|
|
|
ENST00000695691.1:n.1491+133G>T
|
|
|
ENST00000245907.11:c.4630+133G>T
MANE Select
|
ENSP00000245907.4:n.4630+133G>T
|
|
ENST00000245907.10:c.4630+133G>T
|
ENSP00000245907.4:n.4630+133G>T
|
|
ENST00000599668.1:n.250+133G>T
|
|
|
ENST00000599899.5:n.1589+133G>T
|
|
|
ENST00000601008.1:c.242-1034G>T
|
ENSP00000471384.1:n.242-1034G>T
|
|
ENST00000602229.1:c.77+133G>T
|
|
|
NM_000064.3:c.4630+133G>T
|
NP_000055.2:n.4630+133G>T
|
|
NM_000064.4:c.4630+133G>T
MANE Select
|
NP_000055.2:n.4630+133G>T
|
|