ENST00000426263.10:c.973-53G>T
MANE Select
|
ENSP00000416293.2:n.973-53G>T
|
|
ENST00000674545.1:n.414G>T
|
|
|
ENST00000674765.1:c.973-53G>T
|
ENSP00000501811.1:n.973-53G>T
|
|
ENST00000675112.1:n.1274-53G>T
|
|
|
ENST00000676254.1:n.1422-53G>T
|
|
|
ENST00000426263.7:c.973-53G>T
|
ENSP00000416293.2:n.973-53G>T
|
|
ENST00000439722.2:c.852-53G>T
|
ENSP00000395521.2:n.852-53G>T
|
|
ENST00000475162.3:c.415+1540G>T
|
|
|
ENST00000630287.2:c.*288-53G>T
|
ENSP00000486694.1:n.*288-53G>T
|
|
NM_006516.2:c.973-53G>T
|
NP_006507.2:n.973-53G>T
|
|
NM_006516.3:c.973-53G>T
|
NP_006507.2:n.973-53G>T
|
|
NM_006516.4:c.973-53G>T
MANE Select
|
NP_006507.2:n.973-53G>T
|
|