ENST00000496887.7:c.1157+40309G>T
|
ENSP00000434560.2:n.1157+40309G>T
|
|
ENST00000646564.2:c.974+40309G>T
|
ENSP00000495806.2:n.974+40309G>T
|
|
ENST00000155840.12:c.1514+40309G>T
MANE Select
|
ENSP00000155840.2:n.1514+40309G>T
|
|
ENST00000335475.6:c.1133+40309G>T
|
ENSP00000334497.5:n.1133+40309G>T
|
|
ENST00000646564.1:c.620+40309G>T
|
ENSP00000495806.1:n.620+40309G>T
|
|
ENST00000155840.9:c.1514+40309G>T
|
ENSP00000155840.2:n.1514+40309G>T
|
|
ENST00000335475.5:c.1133+40309G>T
|
ENSP00000334497.5:n.1133+40309G>T
|
|
NM_000218.2:c.1514+40309G>T , LRG_287t1:c.1514+40309G>T
|
NP_000209.2:n.1514+40309G>T
|
|
NM_181798.1:c.1133+40309G>T , LRG_287t2:c.1133+40309G>T
|
NP_861463.1:n.1133+40309G>T
|
|
NM_000218.3:c.1514+40309G>T
MANE Select
|
NP_000209.2:n.1514+40309G>T
|
|