ENST00000700555.2:n.483A>T
|
|
|
ENST00000700559.2:c.1980A>T
|
ENSP00000515065.2:p.Gly660=
|
|
ENST00000700563.2:c.1980A>T
|
ENSP00000515066.2:p.Gly660=
|
|
ENST00000546498.2:n.667A>T
|
|
|
ENST00000549461.2:n.519A>T
|
|
|
ENST00000700555.1:c.411A>T
|
ENSP00000515062.1:p.Gly137=
|
|
ENST00000700556.1:c.451A>T
|
|
|
ENST00000700558.1:n.194A>T
|
|
|
ENST00000700559.1:c.1195A>T
|
|
|
ENST00000700560.1:n.1195A>T
|
|
|
ENST00000700561.1:n.1321A>T
|
|
|
ENST00000700562.1:n.518A>T
|
|
|
ENST00000700563.1:c.1934A>T
|
|
|
ENST00000700564.1:n.1984A>T
|
|
|
ENST00000070846.11:c.2112A>T
|
ENSP00000070846.6:p.Gly704=
|
|
ENST00000340811.9:c.1980A>T
MANE Select
|
ENSP00000342800.5:p.Gly660=
|
|
ENST00000070846.10:c.2112A>T
|
ENSP00000070846.6:p.Gly704=
|
|
ENST00000340811.8:c.1980A>T
|
ENSP00000342800.4:p.Gly660=
|
|
ENST00000549461.1:n.426A>T
|
|
|
ENST00000552612.5:n.401A>T
|
|
|
ENST00000613243.1:c.2112A>T
|
ENSP00000478295.1:p.Gly704=
|
|
NM_001005242.2:c.1980A>T
|
NP_001005242.2:p.Gly660=
|
|
NM_004572.3:c.2112A>T , LRG_398t1:c.2112A>T
|
NP_004563.2:p.Gly704=
|
|
NM_001005242.3:c.1980A>T
MANE Select
|
NP_001005242.2:p.Gly660=
|
|
NM_004572.4:c.2112A>T
|
NP_004563.2:p.Gly704=
|
|