ENST00000248846.10:c.2077T>A
MANE Select
|
ENSP00000248846.5:p.Ser693Thr
|
|
ENST00000248846.9:c.2077T>A
|
ENSP00000248846.5:p.Ser693Thr
|
|
ENST00000439308.6:c.2077T>A
|
ENSP00000397387.2:p.Ser693Thr
|
|
ENST00000473946.1:n.386T>A
|
|
|
ENST00000489511.5:n.94T>A
|
|
|
ENST00000491449.5:n.384T>A
|
|
|
ENST00000498611.5:n.2610T>A
|
|
|
NM_020461.3:c.2077T>A
|
NP_065194.2:p.Ser693Thr
|
|
XR_938347.1:n.2642T>A
|
|
|
XR_938348.1:n.2642T>A
|
|
|
XR_001755343.2:n.2646T>A
|
|
|
XR_001755344.2:n.2646T>A
|
|
|
XR_002958720.1:n.2646T>A
|
|
|
XR_938347.2:n.2646T>A
|
|
|
NM_020461.4:c.2077T>A
MANE Select
|
NP_065194.3:p.Ser693Thr
|
|