ENST00000700555.2:n.644G=
|
|
|
ENST00000700557.2:n.233G=
|
|
|
ENST00000700559.2:c.2141G=
|
ENSP00000515065.2:p.Arg714=
|
|
ENST00000546498.2:n.828G=
|
|
|
ENST00000549461.2:n.659+21G=
|
|
|
ENST00000700555.1:c.572G=
|
ENSP00000515062.1:p.Arg191=
|
|
ENST00000700556.1:c.612G=
|
|
|
ENST00000700557.1:c.152G=
|
ENSP00000515064.1:p.Arg51=
|
|
ENST00000700558.1:n.355G=
|
|
|
ENST00000700559.1:c.1356G=
|
|
|
ENST00000700560.1:n.1356G=
|
|
|
ENST00000700561.1:n.1482G=
|
|
|
ENST00000070846.11:c.2273G=
|
ENSP00000070846.6:p.Arg758=
|
|
ENST00000340811.9:c.2141G=
MANE Select
|
ENSP00000342800.5:p.Arg714=
|
|
ENST00000070846.10:c.2273G=
|
ENSP00000070846.6:p.Arg758=
|
|
ENST00000340811.8:c.2141G=
|
ENSP00000342800.4:p.Arg714=
|
|
ENST00000613243.1:c.2273G=
|
ENSP00000478295.1:p.Arg758=
|
|
NM_001005242.2:c.2141G=
|
NP_001005242.2:p.Arg714=
|
|
NM_004572.3:c.2273G= , LRG_398t1:c.2273G=
|
NP_004563.2:p.Arg758=
|
|
NM_001005242.3:c.2141G=
MANE Select
|
NP_001005242.2:p.Arg714=
|
|
NM_004572.4:c.2273G=
|
NP_004563.2:p.Arg758=
|
|