ENST00000261180.10:c.1188+43300T>G
MANE Select
|
ENSP00000261180.5:n.1188+43300T>G
|
|
ENST00000547300.2:c.1188+43300T>G
|
ENSP00000447822.2:n.1188+43300T>G
|
|
ENST00000261180.9:c.1053+43300T>G
|
ENSP00000261180.4:n.1053+43300T>G
|
|
ENST00000261180.8:c.1053+43300T>G
|
ENSP00000261180.4:n.1053+43300T>G
|
|
ENST00000547300.1:c.349+43300T>G
|
|
|
ENST00000548156.1:n.280-47741T>G
|
|
|
NM_013381.2:c.1053+43300T>G
|
NP_037513.1:n.1053+43300T>G
|
|
XM_005268819.3:c.1188+43300T>G
|
XP_005268876.1:n.1188+43300T>G
|
|
XR_944529.1:n.1251+43300T>G
|
|
|
XM_005268819.5:c.1053+43300T>G
|
XP_005268876.2:n.1053+43300T>G
|
|
XM_017019243.2:c.1053+43300T>G
|
XP_016874732.2:n.1053+43300T>G
|
|
XM_017019244.1:c.144+43300T>G
|
XP_016874733.1:n.144+43300T>G
|
|
NM_013381.3:c.1188+43300T>G
MANE Select
|
NP_037513.2:n.1188+43300T>G
|
|