ENST00000675419.1:c.*4238G>T
MANE Select
|
ENSP00000501943.1:n.*4238G>T
|
|
ENST00000300305.7:c.*4238G>T
|
ENSP00000300305.3:n.*4238G>T
|
|
ENST00000344691.8:c.*4238G>T
|
ENSP00000340690.4:n.*4238G>T
|
|
ENST00000437180.5:c.*4238G>T
|
ENSP00000409227.1:n.*4238G>T
|
|
NM_001001890.2:c.*4238G>T
|
NP_001001890.1:n.*4238G>T
|
|
NM_001754.4:c.*4238G>T , LRG_482t1:c.*4238G>T
|
NP_001745.2:n.*4238G>T
|
|
XM_005261068.3:c.*4238G>T
|
XP_005261125.1:n.*4238G>T
|
|
XM_005261069.3:c.*4238G>T
|
XP_005261126.1:n.*4238G>T
|
|
XM_011529766.1:c.*4238G>T
|
XP_011528068.1:n.*4238G>T
|
|
XM_011529767.1:c.*4238G>T
|
XP_011528069.1:n.*4238G>T
|
|
XM_011529768.1:c.*4238G>T
|
XP_011528070.1:n.*4238G>T
|
|
XM_005261069.4:c.*4238G>T
|
XP_005261126.1:n.*4238G>T
|
|
XM_011529766.2:c.*4238G>T
|
XP_011528068.1:n.*4238G>T
|
|
XM_011529767.2:c.*4238G>T
|
XP_011528069.1:n.*4238G>T
|
|
XM_011529768.2:c.*4238G>T
|
XP_011528070.1:n.*4238G>T
|
|
XM_017028487.1:c.*4238G>T
|
XP_016883976.1:n.*4238G>T
|
|
NM_001001890.3:c.*4238G>T
|
NP_001001890.1:n.*4238G>T
|
|
NM_001754.5:c.*4238G>T
MANE Select
|
NP_001745.2:n.*4238G>T
|
|