NM_182895.5:c.1693+312G>C
MANE Select
|
NP_878315.2:n.1693+312G>C
|
ENST00000622235.5:c.1693+312G>C
MANE Select
|
ENSP00000477564.2:n.1693+312G>C
|
NM_153334.6:c.1708+312G>C
|
NP_699165.3:n.1708+312G>C
|
NM_153334.7:c.1708+312G>C
|
NP_699165.3:n.1708+312G>C
|
NM_182895.4:c.1693+312G>C
|
NP_878315.2:n.1693+312G>C
|
ENST00000494535.1:n.584+312G>C
|
|
ENST00000615031.4:c.1708+312G>C
|
ENSP00000479389.1:n.1708+312G>C
|
ENST00000622235.4:c.1693+312G>C
|
ENSP00000477564.1:n.1693+312G>C
|
ENST00000623402.1:c.1708+312G>C
|
ENSP00000485276.1:n.1708+312G>C
|
XM_017029065.2:c.1776+312G>C
|
XP_016884554.1:n.1776+312G>C
|