ENST00000700559.2:c.978A>C
|
ENSP00000515065.2:p.Ala326=
|
|
ENST00000700563.2:c.978A>C
|
ENSP00000515066.2:p.Ala326=
|
|
ENST00000700559.1:c.193A>C
|
|
|
ENST00000700560.1:n.193A>C
|
|
|
ENST00000700561.1:n.319A>C
|
|
|
ENST00000700563.1:c.932A>C
|
|
|
ENST00000700564.1:n.982A>C
|
|
|
ENST00000700565.1:n.831A>C
|
|
|
ENST00000070846.11:c.978A>C
|
ENSP00000070846.6:p.Ala326=
|
|
ENST00000340811.9:c.978A>C
MANE Select
|
ENSP00000342800.5:p.Ala326=
|
|
ENST00000070846.10:c.978A>C
|
ENSP00000070846.6:p.Ala326=
|
|
ENST00000340811.8:c.978A>C
|
ENSP00000342800.4:p.Ala326=
|
|
ENST00000613243.1:c.978A>C
|
ENSP00000478295.1:p.Ala326=
|
|
NM_001005242.2:c.978A>C
|
NP_001005242.2:p.Ala326=
|
|
NM_004572.3:c.978A>C , LRG_398t1:c.978A>C
|
NP_004563.2:p.Ala326=
|
|
NM_001005242.3:c.978A>C
MANE Select
|
NP_001005242.2:p.Ala326=
|
|
NM_004572.4:c.978A>C
|
NP_004563.2:p.Ala326=
|
|