ENST00000449082.3:c.3207T>A
MANE Select
|
ENSP00000390600.2:p.Ser1069=
|
|
ENST00000643924.1:c.3204T>A
|
ENSP00000495595.1:p.Ser1068=
|
|
ENST00000655275.1:c.3231T>A
|
ENSP00000499510.1:p.Ser1077=
|
|
ENST00000449082.2:c.3207T>A
|
ENSP00000390600.2:p.Ser1069=
|
|
NM_001293306.2:c.3204T>A
|
NP_001280235.2:p.Ser1068=
|
|
NM_001293307.2:c.2913T>A
|
NP_001280236.2:p.Ser971=
|
|
NM_006514.3:c.3207T>A
|
NP_006505.3:p.Ser1069=
|
|
XM_005265371.2:c.3216T>A
|
XP_005265428.1:p.Ser1072=
|
|
XM_011533993.1:c.3213T>A
|
XP_011532295.1:p.Ser1071=
|
|
XM_011533994.1:c.2922T>A
|
XP_011532296.1:p.Ser974=
|
|
XM_005265371.3:c.3216T>A
|
XP_005265428.1:p.Ser1072=
|
|
XM_011533993.2:c.3213T>A
|
XP_011532295.1:p.Ser1071=
|
|
XM_011533994.2:c.2922T>A
|
XP_011532296.1:p.Ser974=
|
|
NM_006514.4:c.3207T>A
MANE Select
|
NP_006505.4:p.Ser1069=
|
|