ENST00000358602.9:c.7722C>A
MANE Select
|
ENSP00000351416.4:p.Ser2574=
|
|
ENST00000330838.10:c.6969C>A
|
ENSP00000332265.6:p.Ser2323=
|
|
ENST00000358602.8:c.7722C>A
|
ENSP00000351416.4:p.Ser2574=
|
|
ENST00000509867.6:c.7383C>A
|
ENSP00000427151.2:p.Ser2461=
|
|
ENST00000558247.5:c.7373C>A
|
|
|
NM_001286771.1:c.7383C>A
|
NP_001273700.1:p.Ser2461=
|
|
NM_032217.3:c.7722C>A
|
NP_115593.3:p.Ser2574=
|
|
NM_198889.1:c.6969C>A
|
NP_942592.1:p.Ser2323=
|
|
XM_005265667.3:c.7719C>A
|
XP_005265724.1:p.Ser2573=
|
|
XM_005265671.3:c.6966C>A
|
XP_005265728.1:p.Ser2322=
|
|
NM_001286771.2:c.7383C>A
|
NP_001273700.1:p.Ser2461=
|
|
NM_015574.1:c.7719C>A
|
NP_056389.1:p.Ser2573=
|
|
NM_032217.4:c.7722C>A
|
NP_115593.3:p.Ser2574=
|
|
NM_198889.2:c.6969C>A
|
NP_942592.1:p.Ser2323=
|
|
XM_005265671.4:c.6966C>A
|
XP_005265728.1:p.Ser2322=
|
|
XM_017008011.1:c.7380C>A
|
XP_016863500.1:p.Ser2460=
|
|
XM_017008012.1:c.6630C>A
|
XP_016863501.1:p.Ser2210=
|
|
XM_017008013.1:c.6627C>A
|
XP_016863502.1:p.Ser2209=
|
|
NM_001286771.3:c.7383C>A
|
NP_001273700.1:p.Ser2461=
|
|
NM_015574.2:c.7719C>A
|
NP_056389.1:p.Ser2573=
|
|
NM_032217.5:c.7722C>A
MANE Select
|
NP_115593.3:p.Ser2574=
|
|
NM_198889.3:c.6969C>A
|
NP_942592.1:p.Ser2323=
|
|