ENST00000682028.1:c.1297G=
|
ENSP00000507230.1:p.Val433=
|
|
ENST00000682268.1:n.1595G=
|
|
|
ENST00000682676.1:n.698G=
|
|
|
ENST00000682902.1:n.1599G=
|
|
|
ENST00000683513.1:c.1297G=
|
ENSP00000506809.1:p.Val433=
|
|
ENST00000263431.4:c.1297G=
MANE Select
|
ENSP00000263431.3:p.Val433=
|
|
ENST00000263431.3:c.1297G=
|
ENSP00000263431.3:p.Val433=
|
|
NM_001316329.1:c.1297G=
|
NP_001303258.1:p.Val433=
|
|
NM_002739.3:c.1297G= , LRG_669t1:c.1297G=
|
NP_002730.1:p.Val433=
|
|
NM_002739.4:c.1297G=
|
NP_002730.1:p.Val433=
|
|
XM_011527108.1:c.388G=
|
XP_011525410.1:p.Val130=
|
|
NM_002739.5:c.1297G=
MANE Select
|
NP_002730.1:p.Val433=
|
|
NM_001316329.2:c.1297G=
|
NP_001303258.1:p.Val433=
|
|