ENST00000643794.1:c.-4G>T
|
ENSP00000495765.1:n.-4G>T
|
|
ENST00000651669.1:c.-4G>T
MANE Select
|
ENSP00000499044.1:n.-4G>T
|
|
ENST00000368567.4:c.-4G>T
|
ENSP00000357555.4:n.-4G>T
|
|
ENST00000392558.4:c.-4G>T
|
ENSP00000376341.4:n.-4G>T
|
|
ENST00000477151.1:n.31G>T
|
|
|
ENST00000493224.5:n.31G>T
|
|
|
NM_001030.4:c.-4G>T
|
NP_001021.1:n.-4G>T
|
|
NM_001030.6:c.-4G>T
MANE Select
|
NP_001021.1:n.-4G>T
|
|
NM_001349946.1:c.-221G>T
|
NP_001336875.1:n.-221G>T
|
|
NM_001349947.1:c.-332G>T
|
NP_001336876.1:n.-332G>T
|
|
NM_001349946.2:c.-221G>T
|
NP_001336875.1:n.-221G>T
|
|
NM_001349947.2:c.-332G>T
|
NP_001336876.1:n.-332G>T
|
|