ENST00000449082.3:c.3140G>T
MANE Select
|
ENSP00000390600.2:p.Ser1047Ile
|
|
ENST00000643924.1:c.3137G>T
|
ENSP00000495595.1:p.Ser1046Ile
|
|
ENST00000655275.1:c.3164G>T
|
ENSP00000499510.1:p.Ser1055Ile
|
|
ENST00000449082.2:c.3140G>T
|
ENSP00000390600.2:p.Ser1047Ile
|
|
NM_001293306.2:c.3137G>T
|
NP_001280235.2:p.Ser1046Ile
|
|
NM_001293307.2:c.2846G>T
|
NP_001280236.2:p.Ser949Ile
|
|
NM_006514.3:c.3140G>T
|
NP_006505.3:p.Ser1047Ile
|
|
XM_005265371.2:c.3149G>T
|
XP_005265428.1:p.Ser1050Ile
|
|
XM_011533993.1:c.3146G>T
|
XP_011532295.1:p.Ser1049Ile
|
|
XM_011533994.1:c.2855G>T
|
XP_011532296.1:p.Ser952Ile
|
|
XM_005265371.3:c.3149G>T
|
XP_005265428.1:p.Ser1050Ile
|
|
XM_011533993.2:c.3146G>T
|
XP_011532295.1:p.Ser1049Ile
|
|
XM_011533994.2:c.2855G>T
|
XP_011532296.1:p.Ser952Ile
|
|
NM_006514.4:c.3140G>T
MANE Select
|
NP_006505.4:p.Ser1047Ile
|
|