ENST00000700555.2:n.626T>G
|
|
|
ENST00000700557.2:n.215T>G
|
|
|
ENST00000700559.2:c.2123T>G
|
ENSP00000515065.2:p.Leu708Arg
|
|
ENST00000546498.2:n.810T>G
|
|
|
ENST00000549461.2:n.659+3T>G
|
|
|
ENST00000700555.1:c.554T>G
|
ENSP00000515062.1:p.Leu185Arg
|
|
ENST00000700556.1:c.594T>G
|
|
|
ENST00000700557.1:c.134T>G
|
ENSP00000515064.1:p.Leu45Arg
|
|
ENST00000700558.1:n.337T>G
|
|
|
ENST00000700559.1:c.1338T>G
|
|
|
ENST00000700560.1:n.1338T>G
|
|
|
ENST00000700561.1:n.1464T>G
|
|
|
ENST00000070846.11:c.2255T>G
|
ENSP00000070846.6:p.Leu752Arg
|
|
ENST00000340811.9:c.2123T>G
MANE Select
|
ENSP00000342800.5:p.Leu708Arg
|
|
ENST00000070846.10:c.2255T>G
|
ENSP00000070846.6:p.Leu752Arg
|
|
ENST00000340811.8:c.2123T>G
|
ENSP00000342800.4:p.Leu708Arg
|
|
ENST00000613243.1:c.2255T>G
|
ENSP00000478295.1:p.Leu752Arg
|
|
NM_001005242.2:c.2123T>G
|
NP_001005242.2:p.Leu708Arg
|
|
NM_004572.3:c.2255T>G , LRG_398t1:c.2255T>G
|
NP_004563.2:p.Leu752Arg
|
|
NM_001005242.3:c.2123T>G
MANE Select
|
NP_001005242.2:p.Leu708Arg
|
|
NM_004572.4:c.2255T>G
|
NP_004563.2:p.Leu752Arg
|
|