ENST00000700555.2:n.243G>C
|
|
|
ENST00000700559.2:c.1731G>C
|
ENSP00000515065.2:p.Glu577Asp
|
|
ENST00000700563.2:c.1731G>C
|
ENSP00000515066.2:p.Glu577Asp
|
|
ENST00000546498.2:n.418G>C
|
|
|
ENST00000700555.1:c.171G>C
|
ENSP00000515062.1:p.Glu57Asp
|
|
ENST00000700556.1:c.202G>C
|
|
|
ENST00000700559.1:c.946G>C
|
|
|
ENST00000700560.1:n.946G>C
|
|
|
ENST00000700561.1:n.1072G>C
|
|
|
ENST00000700563.1:c.1685G>C
|
|
|
ENST00000700564.1:n.1735G>C
|
|
|
ENST00000070846.11:c.1863G>C
|
ENSP00000070846.6:p.Glu621Asp
|
|
ENST00000340811.9:c.1731G>C
MANE Select
|
ENSP00000342800.5:p.Glu577Asp
|
|
ENST00000070846.10:c.1863G>C
|
ENSP00000070846.6:p.Glu621Asp
|
|
ENST00000340811.8:c.1731G>C
|
ENSP00000342800.4:p.Glu577Asp
|
|
ENST00000546498.1:n.418G>C
|
|
|
ENST00000552612.5:n.152G>C
|
|
|
ENST00000613243.1:c.1863G>C
|
ENSP00000478295.1:p.Glu621Asp
|
|
NM_001005242.2:c.1731G>C
|
NP_001005242.2:p.Glu577Asp
|
|
NM_004572.3:c.1863G>C , LRG_398t1:c.1863G>C
|
NP_004563.2:p.Glu621Asp
|
|
NM_001005242.3:c.1731G>C
MANE Select
|
NP_001005242.2:p.Glu577Asp
|
|
NM_004572.4:c.1863G>C
|
NP_004563.2:p.Glu621Asp
|
|