ENST00000696142.1:c.*18-278C>G
|
ENSP00000512434.1:n.*18-278C>G
|
|
ENST00000696143.1:c.599+3215C>G
|
ENSP00000512435.1:n.599+3215C>G
|
|
ENST00000696153.1:c.341-278C>G
|
ENSP00000512444.1:n.341-278C>G
|
|
ENST00000256474.3:c.341-278C>G
MANE Select
|
ENSP00000256474.3:n.341-278C>G
|
|
ENST00000256474.2:c.341-278C>G
|
ENSP00000256474.2:n.341-278C>G
|
|
ENST00000345392.2:c.341-3551C>G
|
ENSP00000344757.2:n.341-3551C>G
|
|
ENST00000477538.1:n.477-278C>G
|
|
|
NM_000551.3:c.341-278C>G , LRG_322t1:c.341-278C>G
|
NP_000542.1:n.341-278C>G
|
|
NM_198156.2:c.341-3551C>G
|
NP_937799.1:n.341-3551C>G
|
|
XM_011534078.1:c.*18-278C>G
|
XP_011532380.1:n.*18-278C>G
|
|
NM_001354723.1:c.*17+3215C>G
|
NP_001341652.1:n.*17+3215C>G
|
|
NM_000551.4:c.341-278C>G
MANE Select
|
NP_000542.1:n.341-278C>G
|
|
NM_001354723.2:c.*17+3215C>G
|
NP_001341652.1:n.*17+3215C>G
|
|
NM_198156.3:c.341-3551C>G
|
NP_937799.1:n.341-3551C>G
|
|