ENST00000248846.10:c.3807T>G
MANE Select
|
ENSP00000248846.5:p.His1269Gln
|
|
ENST00000248846.9:c.3807T>G
|
ENSP00000248846.5:p.His1269Gln
|
|
ENST00000439308.6:c.3807T>G
|
ENSP00000397387.2:p.His1269Gln
|
|
ENST00000491449.5:n.2114T>G
|
|
|
ENST00000498611.5:n.3618-537T>G
|
|
|
NM_020461.3:c.3807T>G
|
NP_065194.2:p.His1269Gln
|
|
XR_938347.1:n.4372T>G
|
|
|
XR_938348.1:n.3050-537T>G
|
|
|
XR_001755343.2:n.4376T>G
|
|
|
XR_001755344.2:n.4376T>G
|
|
|
XR_002958720.1:n.3054-537T>G
|
|
|
XR_938347.2:n.4376T>G
|
|
|
NM_020461.4:c.3807T>G
MANE Select
|
NP_065194.3:p.His1269Gln
|
|