ENST00000367002.5:c.*1277G>A
|
ENSP00000355969.4:n.*1277G>A
|
|
ENST00000680073.1:c.*1277G>A
MANE Select
|
ENSP00000505312.1:n.*1277G>A
|
|
ENST00000367002.4:c.*1277G>A
|
ENSP00000355969.4:n.*1277G>A
|
|
ENST00000484910.1:n.1833G>A
|
|
|
NM_001164688.1:c.*1277G>A
|
NP_001158160.1:n.*1277G>A
|
|
NM_183059.2:c.*1277G>A
|
NP_898882.1:n.*1277G>A
|
|
XM_011509479.1:c.*1277G>A
|
XP_011507781.1:n.*1277G>A
|
|
XM_017001151.1:c.*1277G>A
|
XP_016856640.1:n.*1277G>A
|
|
NM_183059.3:c.*1277G>A
|
NP_898882.1:n.*1277G>A
|
|
NM_001164688.2:c.*1277G>A
MANE Select
|
NP_001158160.1:n.*1277G>A
|
|