ENST00000359271.4:c.1396T>A
MANE Select
|
ENSP00000352216.2:p.Phe466Ile
|
|
ENST00000359271.3:c.1396T>A
|
ENSP00000352216.2:p.Phe466Ile
|
|
NM_030777.3:c.1396T>A
|
NP_110404.1:p.Phe466Ile
|
|
XM_011529060.1:c.1459T>A
|
XP_011527362.1:p.Phe487Ile
|
|
XM_011529061.1:c.1405T>A
|
XP_011527363.1:p.Phe469Ile
|
|
XM_011529062.1:c.1508T>A
|
XP_011527364.1:p.Leu503His
|
|
XM_011529063.1:c.1459T>A
|
XP_011527365.1:p.Phe487Ile
|
|
XM_011529064.1:c.1508T>A
|
XP_011527366.1:p.Leu503His
|
|
XM_011529065.1:c.1459T>A
|
XP_011527367.1:p.Phe487Ile
|
|
XR_936641.1:n.1644T>A
|
|
|
XM_011529060.2:c.1459T>A
|
XP_011527362.1:p.Phe487Ile
|
|
XM_011529061.2:c.1405T>A
|
XP_011527363.1:p.Phe469Ile
|
|
XM_011529062.2:c.1508T>A
|
XP_011527364.1:p.Leu503His
|
|
XM_011529063.2:c.1459T>A
|
XP_011527365.1:p.Phe487Ile
|
|
XM_011529064.2:c.1508T>A
|
XP_011527366.1:p.Leu503His
|
|
XM_011529065.2:c.1459T>A
|
XP_011527367.1:p.Phe487Ile
|
|
XM_017028087.2:c.1396T>A
|
XP_016883576.1:p.Phe466Ile
|
|
XR_936641.2:n.1631T>A
|
|
|
NM_030777.4:c.1396T>A
MANE Select
|
NP_110404.1:p.Phe466Ile
|
|