ENST00000682275.1:c.712+16G>C
|
ENSP00000507852.1:n.712+16G>C
|
|
ENST00000683395.1:c.689+16G>C
|
|
|
ENST00000684087.1:c.712+16G>C
|
ENSP00000506978.1:n.712+16G>C
|
|
ENST00000506362.2:c.463+16G>C
|
ENSP00000424103.2:n.463+16G>C
|
|
ENST00000673642.1:c.511+16G>C
|
ENSP00000501242.1:n.511+16G>C
|
|
ENST00000673991.1:c.712+16G>C
|
ENSP00000501033.1:n.712+16G>C
|
|
ENST00000226760.5:c.712+16G>C
MANE Select
|
ENSP00000226760.1:n.712+16G>C
|
|
ENST00000503569.5:c.712+16G>C
|
ENSP00000423337.1:n.712+16G>C
|
|
ENST00000506362.1:c.309+16G>C
|
|
|
ENST00000507765.1:n.897+16G>C
|
|
|
NM_001145853.1:c.712+16G>C
|
NP_001139325.1:n.712+16G>C
|
|
NM_006005.3:c.712+16G>C
MANE Select
|
NP_005996.2:n.712+16G>C
|
|
XM_017008586.1:c.721+16G>C
|
XP_016864075.1:n.721+16G>C
|
|