|
NM_015375.3:c.2349G>T
MANE Select
|
NP_056190.1:p.Val783=
|
|
ENST00000367162.8:c.2349G>T
MANE Select
|
ENSP00000356130.3:p.Val783=
|
|
NM_015375.2:c.2349G>T
|
NP_056190.1:p.Val783=
|
|
NM_199462.2:c.2349G>T
|
NP_955749.1:p.Val783=
|
|
NM_199462.3:c.2349G>T
|
NP_955749.1:p.Val783=
|
|
ENST00000367161.7:c.2349G>T
|
ENSP00000356129.3:p.Val783=
|
|
ENST00000367162.7:c.2349G>T
|
ENSP00000356130.3:p.Val783=
|
|
XM_011509392.1:c.2322G>T
|
XP_011507694.1:p.Val774=
|
|
XM_011509392.2:c.2322G>T
|
XP_011507694.1:p.Val774=
|
|
XM_011509393.1:c.1764G>T
|
XP_011507695.1:p.Val588=
|
|
XM_011509393.2:c.1764G>T
|
XP_011507695.1:p.Val588=
|
|
XM_011509394.1:c.1722G>T
|
XP_011507696.1:p.Val574=
|
|
XM_011509394.2:c.1722G>T
|
XP_011507696.1:p.Val574=
|