ENST00000700555.2:n.631A=
|
|
|
ENST00000700557.2:n.220A=
|
|
|
ENST00000700559.2:c.2128A=
|
ENSP00000515065.2:p.Arg710=
|
|
ENST00000546498.2:n.815A=
|
|
|
ENST00000549461.2:n.659+8A=
|
|
|
ENST00000700555.1:c.559A=
|
ENSP00000515062.1:p.Arg187=
|
|
ENST00000700556.1:c.599A=
|
|
|
ENST00000700557.1:c.139A=
|
ENSP00000515064.1:p.Arg47=
|
|
ENST00000700558.1:n.342A=
|
|
|
ENST00000700559.1:c.1343A=
|
|
|
ENST00000700560.1:n.1343A=
|
|
|
ENST00000700561.1:n.1469A=
|
|
|
ENST00000070846.11:c.2260A=
|
ENSP00000070846.6:p.Arg754=
|
|
ENST00000340811.9:c.2128A=
MANE Select
|
ENSP00000342800.5:p.Arg710=
|
|
ENST00000070846.10:c.2260A=
|
ENSP00000070846.6:p.Arg754=
|
|
ENST00000340811.8:c.2128A=
|
ENSP00000342800.4:p.Arg710=
|
|
ENST00000613243.1:c.2260A=
|
ENSP00000478295.1:p.Arg754=
|
|
NM_001005242.2:c.2128A=
|
NP_001005242.2:p.Arg710=
|
|
NM_004572.3:c.2260A= , LRG_398t1:c.2260A=
|
NP_004563.2:p.Arg754=
|
|
NM_001005242.3:c.2128A=
MANE Select
|
NP_001005242.2:p.Arg710=
|
|
NM_004572.4:c.2260A=
|
NP_004563.2:p.Arg754=
|
|