ENST00000375486.9:c.92+1416_92+1417delinsCT
MANE Select
|
ENSP00000364635.4:n.92+1416_92+1417delinsCT
|
|
ENST00000375481.1:c.92+1416_92+1417delinsCT
|
ENSP00000364630.1:n.92+1416_92+1417delinsCT
|
|
ENST00000375486.8:c.92+1416_92+1417delinsCT
|
ENSP00000364635.4:n.92+1416_92+1417delinsCT
|
|
NM_007365.2:c.92+1416_92+1417delinsCT
|
NP_031391.2:n.92+1416_92+1417delinsCT
|
|
XM_011540549.1:c.92+1416_92+1417delinsCT
|
XP_011538851.1:n.92+1416_92+1417delinsCT
|
|
XR_947004.1:n.4439_4440delinsAG
|
|
|
XR_001736944.1:n.174+1416_174+1417delinsCT
|
|
|
NM_007365.3:c.92+1416_92+1417delinsCT
MANE Select
|
NP_031391.2:n.92+1416_92+1417delinsCT
|
|