ENST00000699980.1:n.225C>G
|
|
|
ENST00000369980.8:c.681C>G
MANE Select
|
ENSP00000358997.3:p.Tyr227Ter
|
|
ENST00000369973.7:c.759C>G
|
ENSP00000358990.3:p.Tyr253Ter
|
|
ENST00000369974.6:c.681C>G
|
ENSP00000358991.2:p.Tyr227Ter
|
|
ENST00000369980.7:c.681C>G
|
ENSP00000358997.3:p.Tyr227Ter
|
|
ENST00000393687.6:c.681C>G
|
ENSP00000377291.2:p.Tyr227Ter
|
|
ENST00000429936.6:c.759C>G
|
ENSP00000392662.2:p.Tyr253Ter
|
|
ENST00000444230.5:c.528+328C>G
|
ENSP00000399974.1:n.528+328C>G
|
|
ENST00000463031.1:n.299C>G
|
|
|
ENST00000477274.1:n.1C>G
|
|
|
NM_001025242.1:c.681C>G
|
NP_001020413.1:p.Tyr227Ter
|
|
NM_001025243.1:c.681C>G
|
NP_001020414.1:p.Tyr227Ter
|
|
NM_001569.3:c.681C>G
|
NP_001560.2:p.Tyr227Ter
|
|
XM_005274668.2:c.759C>G
|
XP_005274725.1:p.Tyr253Ter
|
|
XM_011531158.1:c.681C>G
|
XP_011529460.1:p.Tyr227Ter
|
|
XM_005274668.4:c.759C>G
|
XP_005274725.1:p.Tyr253Ter
|
|
NM_001569.4:c.681C>G
MANE Select
|
NP_001560.2:p.Tyr227Ter
|
|
NM_001025242.2:c.681C>G
|
NP_001020413.1:p.Tyr227Ter
|
|
NM_001025243.2:c.681C>G
|
NP_001020414.1:p.Tyr227Ter
|
|