ENST00000609119.2:c.*3552G>T
|
ENSP00000499659.2:n.*3552G>T
|
|
ENST00000659194.3:c.12448G>T
|
ENSP00000499653.3:p.Glu4150Ter
|
|
ENST00000660292.2:c.12481G>T
|
ENSP00000499787.2:p.Glu4161Ter
|
|
ENST00000659194.2:c.4637G>T
|
|
|
ENST00000366574.7:c.12460G>T
MANE Select
|
ENSP00000355533.2:p.Glu4154Ter
|
|
ENST00000659194.1:c.4637G>T
|
|
|
ENST00000660292.1:c.2513G>T
|
|
|
ENST00000360064.7:c.12412G>T
|
ENSP00000353174.7:p.Glu4138Ter
|
|
ENST00000366574.6:c.12460G>T
|
ENSP00000355533.2:p.Glu4154Ter
|
|
ENST00000609119.1:n.3655G>T
|
|
|
NM_001035.2:c.12460G>T
|
NP_001026.2:p.Glu4154Ter
|
|
XM_006711802.2:c.12514G>T
|
XP_006711865.1:p.Glu4172Ter
|
|
XM_006711803.2:c.12511G>T
|
XP_006711866.1:p.Glu4171Ter
|
|
XM_006711804.2:c.12490G>T
|
XP_006711867.1:p.Glu4164Ter
|
|
XM_006711805.2:c.12484G>T
|
XP_006711868.1:p.Glu4162Ter
|
|
XM_006711806.2:c.12478G>T
|
XP_006711869.1:p.Glu4160Ter
|
|
XM_006711807.2:c.12454G>T
|
XP_006711870.1:p.Glu4152Ter
|
|
XM_006711808.2:c.12277G>T
|
XP_006711871.1:p.Glu4093Ter
|
|
XM_006711810.2:c.12421G>T
|
XP_006711873.1:p.Glu4141Ter
|
|
XM_006711802.3:c.12514G>T
|
XP_006711865.1:p.Glu4172Ter
|
|
XM_006711803.3:c.12511G>T
|
XP_006711866.1:p.Glu4171Ter
|
|
XM_006711804.3:c.12490G>T
|
XP_006711867.1:p.Glu4164Ter
|
|
XM_006711805.3:c.12484G>T
|
XP_006711868.1:p.Glu4162Ter
|
|
XM_006711806.3:c.12478G>T
|
XP_006711869.1:p.Glu4160Ter
|
|
XM_006711807.3:c.12454G>T
|
XP_006711870.1:p.Glu4152Ter
|
|
XM_006711808.3:c.12277G>T
|
XP_006711871.1:p.Glu4093Ter
|
|
XM_006711810.3:c.12421G>T
|
XP_006711873.1:p.Glu4141Ter
|
|
XM_017002028.1:c.12493G>T
|
XP_016857517.1:p.Glu4165Ter
|
|
NM_001035.3:c.12460G>T
MANE Select
|
NP_001026.2:p.Glu4154Ter
|
|