ENST00000594866.3:c.1257G>A
MANE Select
|
ENSP00000469738.2:p.Leu419=
|
|
ENST00000614245.2:c.531G>A
|
ENSP00000480219.2:p.Leu177=
|
|
ENST00000396720.7:c.1257G>A
|
ENSP00000379946.2:p.Leu419=
|
|
ENST00000614245.1:c.1101G>A
|
ENSP00000480219.1:p.Leu367=
|
|
NM_015711.3:c.1257G>A
|
NP_056526.3:p.Leu419=
|
|
XM_005258833.3:c.1257G>A
|
XP_005258890.1:p.Leu419=
|
|
XM_006723180.2:c.1257G>A
|
XP_006723243.1:p.Leu419=
|
|
XM_011526882.1:c.1119G>A
|
XP_011525184.1:p.Leu373=
|
|
XM_011526883.1:c.1257G>A
|
XP_011525185.1:p.Leu419=
|
|
XM_005258833.4:c.1257G>A
|
XP_005258890.1:p.Leu419=
|
|
XM_006723180.3:c.1257G>A
|
XP_006723243.1:p.Leu419=
|
|
XM_011526882.2:c.1119G>A
|
XP_011525184.1:p.Leu373=
|
|
XM_011526883.2:c.1257G>A
|
XP_011525185.1:p.Leu419=
|
|
NM_001394372.1:c.1257G>A
MANE Select
|
NP_001381301.1:p.Leu419=
|
|