ENST00000426263.10:c.516+244C>T
MANE Select
|
ENSP00000416293.2:n.516+244C>T
|
|
ENST00000674765.1:c.516+244C>T
|
ENSP00000501811.1:n.516+244C>T
|
|
ENST00000675112.1:n.539+244C>T
|
|
|
ENST00000676254.1:n.965+244C>T
|
|
|
ENST00000426263.7:c.516+244C>T
|
ENSP00000416293.2:n.516+244C>T
|
|
ENST00000439722.2:c.395+244C>T
|
ENSP00000395521.2:n.395+244C>T
|
|
ENST00000475162.3:c.415+244C>T
|
|
|
ENST00000625233.2:n.968C>T
|
|
|
ENST00000630287.2:c.516+244C>T
|
ENSP00000486694.1:n.516+244C>T
|
|
NM_006516.2:c.516+244C>T
|
NP_006507.2:n.516+244C>T
|
|
NM_006516.3:c.516+244C>T
|
NP_006507.2:n.516+244C>T
|
|
NM_006516.4:c.516+244C>T
MANE Select
|
NP_006507.2:n.516+244C>T
|
|