ENST00000309383.6:c.2118G>T
MANE Select
|
ENSP00000310649.1:p.Val706=
|
|
ENST00000309383.5:c.2118G>T
|
ENSP00000310649.1:p.Val706=
|
|
ENST00000326848.7:c.1203G>T
|
ENSP00000320853.7:p.Val401=
|
|
ENST00000590333.5:c.2166G>T
|
ENSP00000468190.1:p.Val722=
|
|
NM_032430.1:c.2118G>T
|
NP_115806.1:p.Val706=
|
|
XM_005259327.2:c.1848G>T
|
XP_005259384.1:p.Val616=
|
|
XM_011527395.1:c.1875G>T
|
XP_011525697.1:p.Val625=
|
|
XR_430213.2:n.2101G>T
|
|
|
XM_005259327.3:c.1848G>T
|
XP_005259384.1:p.Val616=
|
|
XM_011527395.2:c.1590G>T
|
XP_011525697.2:p.Val530=
|
|
XM_024451739.1:c.1893G>T
|
XP_024307507.1:p.Val631=
|
|
XR_430213.4:n.2399G>T
|
|
|
NM_032430.2:c.2118G>T
MANE Select
|
NP_115806.1:p.Val706=
|
|