ENST00000301061.9:c.1059C>A
MANE Select
|
ENSP00000301061.4:p.His353Gln
|
|
ENST00000301061.8:c.1059C>A
|
ENSP00000301061.4:p.His353Gln
|
|
ENST00000403957.5:c.*341C>A
|
ENSP00000385980.1:n.*341C>A
|
|
ENST00000407467.5:c.*341C>A
|
ENSP00000384691.1:n.*341C>A
|
|
NM_003394.3:c.1059C>A
|
NP_003385.2:p.His353Gln
|
|
XM_011538721.1:c.693C>A
|
XP_011537023.1:p.His231Gln
|
|
XM_011538722.1:c.693C>A
|
XP_011537024.1:p.His231Gln
|
|
XM_011538724.1:c.*337C>A
|
XP_011537026.1:n.*337C>A
|
|
XM_017019919.1:c.693C>A
|
XP_016875408.1:p.His231Gln
|
|
XM_024449179.1:c.693C>A
|
XP_024304947.1:p.His231Gln
|
|
NM_003394.4:c.1059C>A
MANE Select
|
NP_003385.2:p.His353Gln
|
|