ENST00000574538.2:c.1026T>G
MANE Select
|
ENSP00000458290.1:p.Leu342=
|
|
ENST00000319888.10:c.1026T>G
|
ENSP00000320349.6:p.Leu342=
|
|
ENST00000573134.1:n.3327T>G
|
|
|
ENST00000574538.1:c.1026T>G
|
ENSP00000458290.1:p.Leu342=
|
|
ENST00000576251.5:c.221T>G
|
|
|
NM_001308401.1:c.1026T>G
|
NP_001295330.1:p.Leu342=
|
|
NM_022840.3:c.1026T>G
|
NP_073751.3:p.Leu342=
|
|
NM_022840.4:c.1026T>G
|
NP_073751.3:p.Leu342=
|
|
XM_005258132.2:c.1026T>G
|
XP_005258189.1:p.Leu342=
|
|
XM_005258133.1:c.585T>G
|
XP_005258190.1:p.Leu195=
|
|
XM_011525730.1:c.899+5292T>G
|
XP_011524032.1:n.899+5292T>G
|
|
XR_243813.2:n.1549T>G
|
|
|
XM_005258132.4:c.1026T>G
|
XP_005258189.1:p.Leu342=
|
|
XM_005258133.3:c.585T>G
|
XP_005258190.1:p.Leu195=
|
|
XM_011525730.3:c.899+5292T>G
|
XP_011524032.1:n.899+5292T>G
|
|
XR_001753260.2:n.1049T>G
|
|
|
XR_243813.4:n.1740T>G
|
|
|
NM_022840.5:c.1026T>G
MANE Select
|
NP_073751.3:p.Leu342=
|
|
NM_001308401.2:c.1026T>G
|
NP_001295330.1:p.Leu342=
|
|