ENST00000609119.2:c.*3715A>T
|
ENSP00000499659.2:n.*3715A>T
|
|
ENST00000659194.3:c.12611A>T
|
ENSP00000499653.3:p.Glu4204Val
|
|
ENST00000660292.2:c.12644A>T
|
ENSP00000499787.2:p.Glu4215Val
|
|
ENST00000659194.2:c.4800A>T
|
|
|
ENST00000366574.7:c.12623A>T
MANE Select
|
ENSP00000355533.2:p.Glu4208Val
|
|
ENST00000659194.1:c.4800A>T
|
|
|
ENST00000660292.1:c.2676A>T
|
|
|
ENST00000360064.7:c.12575A>T
|
ENSP00000353174.7:p.Glu4192Val
|
|
ENST00000366574.6:c.12623A>T
|
ENSP00000355533.2:p.Glu4208Val
|
|
ENST00000609119.1:n.3818A>T
|
|
|
NM_001035.2:c.12623A>T
|
NP_001026.2:p.Glu4208Val
|
|
XM_006711802.2:c.12677A>T
|
XP_006711865.1:p.Glu4226Val
|
|
XM_006711803.2:c.12674A>T
|
XP_006711866.1:p.Glu4225Val
|
|
XM_006711804.2:c.12653A>T
|
XP_006711867.1:p.Glu4218Val
|
|
XM_006711805.2:c.12647A>T
|
XP_006711868.1:p.Glu4216Val
|
|
XM_006711806.2:c.12641A>T
|
XP_006711869.1:p.Glu4214Val
|
|
XM_006711807.2:c.12617A>T
|
XP_006711870.1:p.Glu4206Val
|
|
XM_006711808.2:c.12440A>T
|
XP_006711871.1:p.Glu4147Val
|
|
XM_006711810.2:c.12584A>T
|
XP_006711873.1:p.Glu4195Val
|
|
XM_006711802.3:c.12677A>T
|
XP_006711865.1:p.Glu4226Val
|
|
XM_006711803.3:c.12674A>T
|
XP_006711866.1:p.Glu4225Val
|
|
XM_006711804.3:c.12653A>T
|
XP_006711867.1:p.Glu4218Val
|
|
XM_006711805.3:c.12647A>T
|
XP_006711868.1:p.Glu4216Val
|
|
XM_006711806.3:c.12641A>T
|
XP_006711869.1:p.Glu4214Val
|
|
XM_006711807.3:c.12617A>T
|
XP_006711870.1:p.Glu4206Val
|
|
XM_006711808.3:c.12440A>T
|
XP_006711871.1:p.Glu4147Val
|
|
XM_006711810.3:c.12584A>T
|
XP_006711873.1:p.Glu4195Val
|
|
XM_017002028.1:c.12656A>T
|
XP_016857517.1:p.Glu4219Val
|
|
NM_001035.3:c.12623A>T
MANE Select
|
NP_001026.2:p.Glu4208Val
|
|