ENST00000257215.10:c.636+773G>A
MANE Select
|
ENSP00000257215.5:n.636+773G>A
|
|
ENST00000257215.9:c.636+773G>A
|
ENSP00000257215.5:n.636+773G>A
|
|
ENST00000540717.1:c.*109+773G>A
|
ENSP00000440264.1:n.*109+773G>A
|
|
NM_006133.2:c.636+773G>A
|
NP_006124.1:n.636+773G>A
|
|
XM_005274230.3:c.636+773G>A
|
XP_005274287.1:n.636+773G>A
|
|
XM_011545235.1:c.636+773G>A
|
XP_011543537.1:n.636+773G>A
|
|
XM_011545236.1:c.636+773G>A
|
XP_011543538.1:n.636+773G>A
|
|
XM_017018238.1:c.636+773G>A
|
XP_016873727.1:n.636+773G>A
|
|
XM_017018239.1:c.636+773G>A
|
XP_016873728.1:n.636+773G>A
|
|
XM_017018240.1:c.636+773G>A
|
XP_016873729.1:n.636+773G>A
|
|
NM_006133.3:c.636+773G>A
MANE Select
|
NP_006124.1:n.636+773G>A
|
|