ENST00000703783.1:n.2950+414G>C
|
|
|
ENST00000703785.1:n.2869+414G>C
|
|
|
ENST00000262464.9:c.6166+414G>C
MANE Select
|
ENSP00000262464.4:n.6166+414G>C
|
|
ENST00000262464.8:c.6166+414G>C
|
ENSP00000262464.4:n.6166+414G>C
|
|
ENST00000508053.5:c.6166+414G>C
|
ENSP00000424571.1:n.6166+414G>C
|
|
ENST00000619499.4:c.6163+414G>C
|
ENSP00000482132.1:n.6163+414G>C
|
|
NM_001999.3:c.6166+414G>C
|
NP_001990.2:n.6166+414G>C
|
|
XM_017009228.2:c.6013+414G>C
|
XP_016864717.1:n.6013+414G>C
|
|
NM_001999.4:c.6166+414G>C
MANE Select
|
NP_001990.2:n.6166+414G>C
|
|