ENST00000394329.9:c.14844T>A
MANE Select
|
ENSP00000377862.4:p.Val4948=
|
|
ENST00000674496.2:c.9615T>A
|
ENSP00000501473.2:p.Val3205=
|
|
ENST00000335110.5:c.9561T>A
|
ENSP00000335169.5:p.Val3187=
|
|
ENST00000394329.7:c.14838T>A
|
ENSP00000377862.3:p.Val4946=
|
|
NM_001291285.1:c.14841T>A
|
NP_001278214.1:p.Val4947=
|
|
NM_001291303.1:c.14844T>A
|
NP_001278232.1:p.Val4948=
|
|
NM_024582.4:c.14838T>A
|
NP_078858.4:p.Val4946=
|
|
XM_011532236.1:c.14844T>A
|
XP_011530538.1:p.Val4948=
|
|
XM_011532237.1:c.9615T>A
|
XP_011530539.1:p.Val3205=
|
|
XM_011532236.2:c.14844T>A
|
XP_011530538.1:p.Val4948=
|
|
XM_011532237.2:c.9615T>A
|
XP_011530539.1:p.Val3205=
|
|
NM_001291285.2:c.14841T>A
|
NP_001278214.1:p.Val4947=
|
|
NM_001291303.3:c.14844T>A
MANE Select
|
NP_001278232.1:p.Val4948=
|
|
NM_024582.5:c.14838T>A
|
NP_078858.4:p.Val4946=
|
|
NM_001291285.3:c.14841T>A
|
NP_001278214.1:p.Val4947=
|
|
NM_024582.6:c.14838T>A
|
NP_078858.4:p.Val4946=
|
|