ENST00000696142.1:c.*18-263G>T
|
ENSP00000512434.1:n.*18-263G>T
|
|
ENST00000696143.1:c.599+3230G>T
|
ENSP00000512435.1:n.599+3230G>T
|
|
ENST00000696153.1:c.341-263G>T
|
ENSP00000512444.1:n.341-263G>T
|
|
ENST00000256474.3:c.341-263G>T
MANE Select
|
ENSP00000256474.3:n.341-263G>T
|
|
ENST00000256474.2:c.341-263G>T
|
ENSP00000256474.2:n.341-263G>T
|
|
ENST00000345392.2:c.341-3536G>T
|
ENSP00000344757.2:n.341-3536G>T
|
|
ENST00000477538.1:n.477-263G>T
|
|
|
NM_000551.3:c.341-263G>T , LRG_322t1:c.341-263G>T
|
NP_000542.1:n.341-263G>T
|
|
NM_198156.2:c.341-3536G>T
|
NP_937799.1:n.341-3536G>T
|
|
XM_011534078.1:c.*18-263G>T
|
XP_011532380.1:n.*18-263G>T
|
|
NM_001354723.1:c.*17+3230G>T
|
NP_001341652.1:n.*17+3230G>T
|
|
NM_000551.4:c.341-263G>T
MANE Select
|
NP_000542.1:n.341-263G>T
|
|
NM_001354723.2:c.*17+3230G>T
|
NP_001341652.1:n.*17+3230G>T
|
|
NM_198156.3:c.341-3536G>T
|
NP_937799.1:n.341-3536G>T
|
|