ENST00000496887.7:c.1233+214G=
|
ENSP00000434560.2:n.1233+214G=
|
|
ENST00000646564.2:c.1050+214G=
|
ENSP00000495806.2:n.1050+214G=
|
|
ENST00000155840.12:c.1590+214G=
MANE Select
|
ENSP00000155840.2:n.1590+214G=
|
|
ENST00000335475.6:c.1209+214G=
|
ENSP00000334497.5:n.1209+214G=
|
|
ENST00000646564.1:c.696+214G=
|
ENSP00000495806.1:n.696+214G=
|
|
ENST00000155840.9:c.1590+214G=
|
ENSP00000155840.2:n.1590+214G=
|
|
ENST00000335475.5:c.1209+214G=
|
ENSP00000334497.5:n.1209+214G=
|
|
NM_000218.2:c.1590+214G= , LRG_287t1:c.1590+214G=
|
NP_000209.2:n.1590+214G=
|
|
NM_181798.1:c.1209+214G= , LRG_287t2:c.1209+214G=
|
NP_861463.1:n.1209+214G=
|
|
NM_000218.3:c.1590+214G=
MANE Select
|
NP_000209.2:n.1590+214G=
|
|