ENST00000426263.10:c.516+234G>C
MANE Select
|
ENSP00000416293.2:n.516+234G>C
|
|
ENST00000674765.1:c.516+234G>C
|
ENSP00000501811.1:n.516+234G>C
|
|
ENST00000675112.1:n.539+234G>C
|
|
|
ENST00000676254.1:n.965+234G>C
|
|
|
ENST00000426263.7:c.516+234G>C
|
ENSP00000416293.2:n.516+234G>C
|
|
ENST00000439722.2:c.395+234G>C
|
ENSP00000395521.2:n.395+234G>C
|
|
ENST00000475162.3:c.415+234G>C
|
|
|
ENST00000625233.2:n.958G>C
|
|
|
ENST00000630287.2:c.516+234G>C
|
ENSP00000486694.1:n.516+234G>C
|
|
NM_006516.2:c.516+234G>C
|
NP_006507.2:n.516+234G>C
|
|
NM_006516.3:c.516+234G>C
|
NP_006507.2:n.516+234G>C
|
|
NM_006516.4:c.516+234G>C
MANE Select
|
NP_006507.2:n.516+234G>C
|
|