ENST00000223051.8:c.810G>A
MANE Select
|
ENSP00000223051.3:p.Leu270=
|
|
ENST00000223051.7:c.810G>A
|
ENSP00000223051.3:p.Leu270=
|
|
ENST00000431692.5:c.810G>A
|
ENSP00000413905.1:p.Leu270=
|
|
ENST00000462090.5:n.51G>A
|
|
|
ENST00000462107.1:c.810G>A
|
ENSP00000420525.1:p.Leu270=
|
|
ENST00000465294.5:n.815G>A
|
|
|
ENST00000473374.5:n.260G>A
|
|
|
ENST00000473571.1:n.264G>A
|
|
|
ENST00000475011.1:n.339G>A
|
|
|
ENST00000476304.5:n.431G>A
|
|
|
ENST00000490084.5:c.65G>A
|
|
|
NM_001206855.1:c.297G>A
|
NP_001193784.1:p.Leu99=
|
|
NM_003227.3:c.810G>A
|
NP_003218.2:p.Leu270=
|
|
XM_005250553.3:c.810G>A
|
XP_005250610.1:p.Leu270=
|
|
XM_005250554.3:c.810G>A
|
XP_005250611.1:p.Leu270=
|
|
NM_001206855.2:c.297G>A
|
NP_001193784.1:p.Leu99=
|
|
XM_005250553.4:c.810G>A
|
XP_005250610.1:p.Leu270=
|
|
XM_017012573.1:c.810G>A
|
XP_016868062.1:p.Leu270=
|
|
NM_003227.4:c.810G>A
MANE Select
|
NP_003218.2:p.Leu270=
|
|
NM_001206855.3:c.297G>A
|
NP_001193784.1:p.Leu99=
|
|