ENST00000609119.2:c.*3592A>T
|
ENSP00000499659.2:n.*3592A>T
|
|
ENST00000659194.3:c.12488A>T
|
ENSP00000499653.3:p.Glu4163Val
|
|
ENST00000660292.2:c.12521A>T
|
ENSP00000499787.2:p.Glu4174Val
|
|
ENST00000659194.2:c.4677A>T
|
|
|
ENST00000366574.7:c.12500A>T
MANE Select
|
ENSP00000355533.2:p.Glu4167Val
|
|
ENST00000659194.1:c.4677A>T
|
|
|
ENST00000660292.1:c.2553A>T
|
|
|
ENST00000360064.7:c.12452A>T
|
ENSP00000353174.7:p.Glu4151Val
|
|
ENST00000366574.6:c.12500A>T
|
ENSP00000355533.2:p.Glu4167Val
|
|
ENST00000609119.1:n.3695A>T
|
|
|
NM_001035.2:c.12500A>T
|
NP_001026.2:p.Glu4167Val
|
|
XM_006711802.2:c.12554A>T
|
XP_006711865.1:p.Glu4185Val
|
|
XM_006711803.2:c.12551A>T
|
XP_006711866.1:p.Glu4184Val
|
|
XM_006711804.2:c.12530A>T
|
XP_006711867.1:p.Glu4177Val
|
|
XM_006711805.2:c.12524A>T
|
XP_006711868.1:p.Glu4175Val
|
|
XM_006711806.2:c.12518A>T
|
XP_006711869.1:p.Glu4173Val
|
|
XM_006711807.2:c.12494A>T
|
XP_006711870.1:p.Glu4165Val
|
|
XM_006711808.2:c.12317A>T
|
XP_006711871.1:p.Glu4106Val
|
|
XM_006711810.2:c.12461A>T
|
XP_006711873.1:p.Glu4154Val
|
|
XM_006711802.3:c.12554A>T
|
XP_006711865.1:p.Glu4185Val
|
|
XM_006711803.3:c.12551A>T
|
XP_006711866.1:p.Glu4184Val
|
|
XM_006711804.3:c.12530A>T
|
XP_006711867.1:p.Glu4177Val
|
|
XM_006711805.3:c.12524A>T
|
XP_006711868.1:p.Glu4175Val
|
|
XM_006711806.3:c.12518A>T
|
XP_006711869.1:p.Glu4173Val
|
|
XM_006711807.3:c.12494A>T
|
XP_006711870.1:p.Glu4165Val
|
|
XM_006711808.3:c.12317A>T
|
XP_006711871.1:p.Glu4106Val
|
|
XM_006711810.3:c.12461A>T
|
XP_006711873.1:p.Glu4154Val
|
|
XM_017002028.1:c.12533A>T
|
XP_016857517.1:p.Glu4178Val
|
|
NM_001035.3:c.12500A>T
MANE Select
|
NP_001026.2:p.Glu4167Val
|
|