ENST00000700555.2:n.207C>T
|
|
|
ENST00000700559.2:c.1695C>T
|
ENSP00000515065.2:p.Cys565=
|
|
ENST00000700563.2:c.1695C>T
|
ENSP00000515066.2:p.Cys565=
|
|
ENST00000546498.2:n.382C>T
|
|
|
ENST00000700555.1:c.135C>T
|
ENSP00000515062.1:p.Cys45=
|
|
ENST00000700556.1:c.166C>T
|
|
|
ENST00000700559.1:c.910C>T
|
|
|
ENST00000700560.1:n.910C>T
|
|
|
ENST00000700561.1:n.1036C>T
|
|
|
ENST00000700563.1:c.1649C>T
|
|
|
ENST00000700564.1:n.1699C>T
|
|
|
ENST00000070846.11:c.1827C>T
|
ENSP00000070846.6:p.Cys609=
|
|
ENST00000340811.9:c.1695C>T
MANE Select
|
ENSP00000342800.5:p.Cys565=
|
|
ENST00000070846.10:c.1827C>T
|
ENSP00000070846.6:p.Cys609=
|
|
ENST00000340811.8:c.1695C>T
|
ENSP00000342800.4:p.Cys565=
|
|
ENST00000546498.1:n.382C>T
|
|
|
ENST00000552612.5:n.116C>T
|
|
|
ENST00000613243.1:c.1827C>T
|
ENSP00000478295.1:p.Cys609=
|
|
NM_001005242.2:c.1695C>T
|
NP_001005242.2:p.Cys565=
|
|
NM_004572.3:c.1827C>T , LRG_398t1:c.1827C>T
|
NP_004563.2:p.Cys609=
|
|
NM_001005242.3:c.1695C>T
MANE Select
|
NP_001005242.2:p.Cys565=
|
|
NM_004572.4:c.1827C>T
|
NP_004563.2:p.Cys609=
|
|