ENST00000457135.2:c.1645T>A
|
|
|
ENST00000334344.11:c.5379T>A
MANE Select
|
ENSP00000335044.6:p.His1793Gln
|
|
ENST00000334344.10:c.5379T>A
|
ENSP00000335044.6:p.His1793Gln
|
|
ENST00000444670.5:c.4209T>A
|
ENSP00000397307.1:p.His1403Gln
|
|
ENST00000457135.1:c.*54T>A
|
ENSP00000388357.1:n.*54T>A
|
|
ENST00000479608.5:n.4670T>A
|
|
|
NM_152641.2:c.5379T>A
|
NP_689854.2:p.His1793Gln
|
|
XM_006719272.2:c.*54T>A
|
XP_006719335.1:n.*54T>A
|
|
XM_011538025.1:c.3747T>A
|
XP_011536327.1:p.His1249Gln
|
|
XR_944505.1:n.5585T>A
|
|
|
NM_152641.3:c.5379T>A
|
NP_689854.2:p.His1793Gln
|
|
XM_006719272.4:c.*54T>A
|
XP_006719335.1:n.*54T>A
|
|
XR_944505.3:n.5568T>A
|
|
|
NM_152641.4:c.5379T>A
MANE Select
|
NP_689854.2:p.His1793Gln
|
|