ENST00000502773.6:c.495+11838T>A
MANE Select
|
ENSP00000422464.1:n.495+11838T>A
|
|
ENST00000274071.6:c.*403+11838T>A
|
ENSP00000274071.2:n.*403+11838T>A
|
|
ENST00000422544.2:c.495+11838T>A
|
ENSP00000410048.2:n.495+11838T>A
|
|
ENST00000502773.5:c.495+11838T>A
|
ENSP00000422464.1:n.495+11838T>A
|
|
ENST00000506880.5:c.149+11838T>A
|
|
|
ENST00000511985.1:n.55+11838T>A
|
|
|
ENST00000512711.1:n.418-26106T>A
|
|
|
NM_016205.2:c.495+11838T>A
|
NP_057289.1:n.495+11838T>A
|
|
NR_036641.1:n.1047+11838T>A
|
|
|
XM_011532124.1:c.462+11838T>A
|
XP_011530426.1:n.462+11838T>A
|
|
XM_011532125.1:c.426+11838T>A
|
XP_011530427.1:n.426+11838T>A
|
|
XM_011532124.2:c.462+11838T>A
|
XP_011530426.1:n.462+11838T>A
|
|
XM_017008455.1:c.390+11838T>A
|
XP_016863944.1:n.390+11838T>A
|
|
XM_017008456.2:c.495+11838T>A
|
XP_016863945.1:n.495+11838T>A
|
|
NM_016205.3:c.495+11838T>A
MANE Select
|
NP_057289.1:n.495+11838T>A
|
|
NR_036641.2:n.1452+11838T>A
|
|
|