ENST00000248846.10:c.3893C>A
MANE Select
|
ENSP00000248846.5:p.Pro1298His
|
|
ENST00000248846.9:c.3893C>A
|
ENSP00000248846.5:p.Pro1298His
|
|
ENST00000439308.6:c.3893C>A
|
ENSP00000397387.2:p.Pro1298His
|
|
ENST00000491449.5:n.2200C>A
|
|
|
ENST00000498611.5:n.3618-451C>A
|
|
|
NM_020461.3:c.3893C>A
|
NP_065194.2:p.Pro1298His
|
|
XR_938347.1:n.4458C>A
|
|
|
XR_938348.1:n.3050-451C>A
|
|
|
XR_001755343.2:n.4462C>A
|
|
|
XR_001755344.2:n.4462C>A
|
|
|
XR_002958720.1:n.3054-451C>A
|
|
|
XR_938347.2:n.4462C>A
|
|
|
NM_020461.4:c.3893C>A
MANE Select
|
NP_065194.3:p.Pro1298His
|
|