ENST00000700555.2:n.660G>C
|
|
|
ENST00000700557.2:n.249G>C
|
|
|
ENST00000700559.2:c.2157G>C
|
ENSP00000515065.2:p.Gln719His
|
|
ENST00000546498.2:n.844G>C
|
|
|
ENST00000549461.2:n.659+37G>C
|
|
|
ENST00000700555.1:c.588G>C
|
ENSP00000515062.1:p.Gln196His
|
|
ENST00000700556.1:c.628G>C
|
|
|
ENST00000700557.1:c.168G>C
|
ENSP00000515064.1:p.Gln56His
|
|
ENST00000700558.1:n.371G>C
|
|
|
ENST00000700559.1:c.1372G>C
|
|
|
ENST00000700560.1:n.1372G>C
|
|
|
ENST00000700561.1:n.1498G>C
|
|
|
ENST00000070846.11:c.2289G>C
|
ENSP00000070846.6:p.Gln763His
|
|
ENST00000340811.9:c.2157G>C
MANE Select
|
ENSP00000342800.5:p.Gln719His
|
|
ENST00000070846.10:c.2289G>C
|
ENSP00000070846.6:p.Gln763His
|
|
ENST00000340811.8:c.2157G>C
|
ENSP00000342800.4:p.Gln719His
|
|
ENST00000613243.1:c.2289G>C
|
ENSP00000478295.1:p.Gln763His
|
|
NM_001005242.2:c.2157G>C
|
NP_001005242.2:p.Gln719His
|
|
NM_004572.3:c.2289G>C , LRG_398t1:c.2289G>C
|
NP_004563.2:p.Gln763His
|
|
NM_001005242.3:c.2157G>C
MANE Select
|
NP_001005242.2:p.Gln719His
|
|
NM_004572.4:c.2289G>C
|
NP_004563.2:p.Gln763His
|
|