ENST00000700555.2:n.699C>T
|
|
|
ENST00000700557.2:n.288C>T
|
|
|
ENST00000700559.2:c.2168-3539C>T
|
ENSP00000515065.2:n.2168-3539C>T
|
|
ENST00000546498.2:n.883C>T
|
|
|
ENST00000549461.2:n.688C>T
|
|
|
ENST00000700555.1:c.627C>T
|
ENSP00000515062.1:p.Ser209=
|
|
ENST00000700556.1:c.667C>T
|
|
|
ENST00000700557.1:c.207C>T
|
ENSP00000515064.1:p.Ser69=
|
|
ENST00000700558.1:n.410C>T
|
|
|
ENST00000700559.1:c.1383-3539C>T
|
|
|
ENST00000700560.1:n.1411C>T
|
|
|
ENST00000700561.1:n.1537C>T
|
|
|
ENST00000070846.11:c.2328C>T
|
ENSP00000070846.6:p.Ser776=
|
|
ENST00000340811.9:c.2196C>T
MANE Select
|
ENSP00000342800.5:p.Ser732=
|
|
ENST00000070846.10:c.2328C>T
|
ENSP00000070846.6:p.Ser776=
|
|
ENST00000340811.8:c.2196C>T
|
ENSP00000342800.4:p.Ser732=
|
|
ENST00000613243.1:c.2328C>T
|
ENSP00000478295.1:p.Ser776=
|
|
NM_001005242.2:c.2196C>T
|
NP_001005242.2:p.Ser732=
|
|
NM_004572.3:c.2328C>T , LRG_398t1:c.2328C>T
|
NP_004563.2:p.Ser776=
|
|
NM_001005242.3:c.2196C>T
MANE Select
|
NP_001005242.2:p.Ser732=
|
|
NM_004572.4:c.2328C>T
|
NP_004563.2:p.Ser776=
|
|