ENST00000248846.10:c.3875G>C
MANE Select
|
ENSP00000248846.5:p.Arg1292Thr
|
|
ENST00000248846.9:c.3875G>C
|
ENSP00000248846.5:p.Arg1292Thr
|
|
ENST00000439308.6:c.3875G>C
|
ENSP00000397387.2:p.Arg1292Thr
|
|
ENST00000491449.5:n.2182G>C
|
|
|
ENST00000498611.5:n.3618-469G>C
|
|
|
NM_020461.3:c.3875G>C
|
NP_065194.2:p.Arg1292Thr
|
|
XR_938347.1:n.4440G>C
|
|
|
XR_938348.1:n.3050-469G>C
|
|
|
XR_001755343.2:n.4444G>C
|
|
|
XR_001755344.2:n.4444G>C
|
|
|
XR_002958720.1:n.3054-469G>C
|
|
|
XR_938347.2:n.4444G>C
|
|
|
NM_020461.4:c.3875G>C
MANE Select
|
NP_065194.3:p.Arg1292Thr
|
|