ENST00000216468.8:c.*2755A>G
MANE Select
|
ENSP00000216468.7:n.*2755A>G
|
|
ENST00000216468.7:c.*2755A>G
|
ENSP00000216468.7:n.*2755A>G
|
|
XM_005267544.3:c.*2755A>G
|
XP_005267601.1:n.*2755A>G
|
|
NM_001346131.1:c.*2755A>G
|
NP_001333060.1:n.*2755A>G
|
|
NM_001346133.1:c.*2755A>G
|
NP_001333062.1:n.*2755A>G
|
|
NM_001346134.1:c.*2755A>G
|
NP_001333063.1:n.*2755A>G
|
|
NM_213601.2:c.*2755A>G
|
NP_998766.1:n.*2755A>G
|
|
XM_017021224.1:c.*2755A>G
|
XP_016876713.1:n.*2755A>G
|
|
NM_213601.3:c.*2755A>G
MANE Select
|
NP_998766.1:n.*2755A>G
|
|
NM_001346131.2:c.*2755A>G
|
NP_001333060.1:n.*2755A>G
|
|
NM_001346133.2:c.*2755A>G
|
NP_001333062.1:n.*2755A>G
|
|