ENST00000374479.4:c.1044T>A
MANE Select
|
ENSP00000363603.3:p.Val348=
|
|
ENST00000374479.3:c.1044T>A
|
ENSP00000363603.3:p.Val348=
|
|
NM_000147.4:c.1044T>A
|
NP_000138.2:p.Val348=
|
|
XM_005245821.1:c.669T>A
|
XP_005245878.1:p.Val223=
|
|
XM_011541167.1:c.411T>A
|
XP_011539469.1:p.Val137=
|
|
XM_005245821.3:c.669T>A
|
XP_005245878.1:p.Val223=
|
|
XM_011541167.3:c.411T>A
|
XP_011539469.1:p.Val137=
|
|
XM_017000905.2:c.741T>A
|
XP_016856394.1:p.Val247=
|
|
NM_000147.5:c.1044T>A
MANE Select
|
NP_000138.2:p.Val348=
|
|
NR_174379.1:n.1222T>A
|
|
|
NR_174380.1:n.1271T>A
|
|
|
NR_174381.1:n.1110T>A
|
|
|
NR_174382.1:n.1507T>A
|
|
|