ENST00000286657.10:c.1725A>G
MANE Select
|
ENSP00000286657.4:p.Thr575=
|
|
ENST00000286657.8:c.1725A>G
|
ENSP00000286657.4:p.Thr575=
|
|
ENST00000622135.1:c.1725A>G
|
ENSP00000480055.1:p.Thr575=
|
|
NM_014243.2:c.1725A>G
|
NP_055058.2:p.Thr575=
|
|
XM_011532421.1:c.1668A>G
|
XP_011530723.1:p.Thr556=
|
|
XM_011532422.1:c.1641A>G
|
XP_011530724.1:p.Thr547=
|
|
XM_011532423.1:c.1083A>G
|
XP_011530725.1:p.Thr361=
|
|
XM_011532424.1:c.993A>G
|
XP_011530726.1:p.Thr331=
|
|
XM_011532421.2:c.1668A>G
|
XP_011530723.1:p.Thr556=
|
|
XM_011532422.3:c.1641A>G
|
XP_011530724.1:p.Thr547=
|
|
NM_014243.3:c.1725A>G
MANE Select
|
NP_055058.2:p.Thr575=
|
|