ENST00000367651.4:c.753C>T
MANE Select
|
ENSP00000356623.2:p.Asn251=
|
|
ENST00000367651.3:c.753C>T
|
ENSP00000356623.2:p.Asn251=
|
|
ENST00000536159.2:c.753C>T
|
ENSP00000442831.1:p.Asn251=
|
|
ENST00000537332.2:c.768C>T
|
ENSP00000444198.2:p.Asn256=
|
|
ENST00000618718.1:c.582C>T
|
ENSP00000479918.1:p.Asn194=
|
|
NM_001168388.2:c.753C>T
|
NP_001161860.1:p.Asn251=
|
|
NM_001168389.2:c.768C>T
|
NP_001161861.2:p.Asn256=
|
|
NM_006079.4:c.753C>T
|
NP_006070.2:p.Asn251=
|
|
NM_006079.5:c.753C>T
MANE Select
|
NP_006070.2:p.Asn251=
|
|
NM_001168388.3:c.753C>T
|
NP_001161860.1:p.Asn251=
|
|
NM_001168389.3:c.768C>T
|
NP_001161861.2:p.Asn256=
|
|