ENST00000517746.6:c.*1414A>T
MANE Select
|
ENSP00000428340.1:n.*1414A>T
|
|
ENST00000297450.7:c.*1414A>T
|
ENSP00000297450.3:n.*1414A>T
|
|
ENST00000517746.5:c.*1414A>T
|
ENSP00000428340.1:n.*1414A>T
|
|
NM_001146.3:c.*1414A>T
|
NP_001137.2:n.*1414A>T
|
|
NM_001146.4:c.*1414A>T
|
NP_001137.2:n.*1414A>T
|
|
NM_001199859.1:c.*1414A>T
|
NP_001186788.1:n.*1414A>T
|
|
NM_001199859.2:c.*1414A>T
|
NP_001186788.1:n.*1414A>T
|
|
NM_001314051.1:c.*1414A>T
|
NP_001300980.1:n.*1414A>T
|
|
XR_928319.1:n.3196A>T
|
|
|
XR_928319.2:n.2811A>T
|
|
|
NM_001146.5:c.*1414A>T
MANE Select
|
NP_001137.2:n.*1414A>T
|
|
NM_001199859.3:c.*1414A>T
|
NP_001186788.1:n.*1414A>T
|
|
NM_001314051.2:c.*1414A>T
|
NP_001300980.1:n.*1414A>T
|
|