ENST00000374479.4:c.1042G=
MANE Select
|
ENSP00000363603.3:p.Val348=
|
|
ENST00000374479.3:c.1042G=
|
ENSP00000363603.3:p.Val348=
|
|
NM_000147.4:c.1042G=
|
NP_000138.2:p.Val348=
|
|
XM_005245821.1:c.667G=
|
XP_005245878.1:p.Val223=
|
|
XM_011541167.1:c.409G=
|
XP_011539469.1:p.Val137=
|
|
XM_005245821.3:c.667G=
|
XP_005245878.1:p.Val223=
|
|
XM_011541167.3:c.409G=
|
XP_011539469.1:p.Val137=
|
|
XM_017000905.2:c.739G=
|
XP_016856394.1:p.Val247=
|
|
NM_000147.5:c.1042G=
MANE Select
|
NP_000138.2:p.Val348=
|
|
NR_174379.1:n.1220G=
|
|
|
NR_174380.1:n.1269G=
|
|
|
NR_174381.1:n.1108G=
|
|
|
NR_174382.1:n.1505G=
|
|
|