|
NM_001985.3:c.216+1G>C
MANE Select
|
NP_001976.1:n.216+1G>C
|
|
ENST00000309244.9:c.216+1G>C
MANE Select
|
ENSP00000311930.3:n.216+1G>C
|
|
NM_001014763.1:c.489+1G>C
|
NP_001014763.1:n.489+1G>C
|
|
NM_001985.2:c.216+1G>C
|
NP_001976.1:n.216+1G>C
|
|
ENST00000309244.8:c.216+1G>C
|
ENSP00000311930.3:n.216+1G>C
|
|
ENST00000354232.8:c.489+1G>C
|
ENSP00000346173.3:n.489+1G>C
|
|
ENST00000593992.1:n.239+1G>C
|
|
|
ENST00000596253.1:c.216+1G>C
|
ENSP00000469628.1:n.216+1G>C
|
|
ENST00000600067.1:c.*142+1G>C
|
ENSP00000469452.1:n.*142+1G>C
|
|
XM_024451418.1:c.105+1G>C
|
XP_024307186.1:n.105+1G>C
|