ENST00000344408.10:c.2618C>T
MANE Select
|
ENSP00000342144.5:p.Ala873Val
|
|
ENST00000310917.6:c.2378C>T
|
ENSP00000311683.2:p.Ala793Val
|
|
ENST00000344408.9:c.2618C>T
|
ENSP00000342144.5:p.Ala873Val
|
|
ENST00000475313.5:c.2378C>T
|
ENSP00000431981.1:p.Ala793Val
|
|
ENST00000509670.1:c.*1011C>T
|
ENSP00000423876.1:n.*1011C>T
|
|
NM_001166136.1:c.2378C>T
|
NP_001159608.1:p.Ala793Val
|
|
NM_147127.4:c.2618C>T
|
NP_667338.3:p.Ala873Val
|
|
XM_011513392.1:c.2627C>T
|
XP_011511694.1:p.Ala876Val
|
|
XM_011513393.1:c.2627C>T
|
XP_011511695.1:p.Ala876Val
|
|
XM_011513394.1:c.2387C>T
|
XP_011511696.1:p.Ala796Val
|
|
XM_017007736.1:c.2378C>T
|
XP_016863225.1:p.Ala793Val
|
|
XM_017007737.1:c.2378C>T
|
XP_016863226.1:p.Ala793Val
|
|
XM_017007738.1:c.2618C>T
|
XP_016863227.1:p.Ala873Val
|
|
XM_017007739.1:c.938C>T
|
XP_016863228.1:p.Ala313Val
|
|
XM_024453893.1:c.938C>T
|
XP_024309661.1:p.Ala313Val
|
|
XR_001741141.1:n.2683C>T
|
|
|
NM_147127.5:c.2618C>T
MANE Select
|
NP_667338.3:p.Ala873Val
|
|
NM_001166136.2:c.2378C>T
|
NP_001159608.1:p.Ala793Val
|
|