ENST00000394817.7:c.1317T>A
MANE Select
|
ENSP00000378294.2:p.Asp439Glu
|
|
ENST00000265195.9:c.1317T>A
|
ENSP00000265195.5:p.Asp439Glu
|
|
ENST00000394817.6:c.1317T>A
|
ENSP00000378294.2:p.Asp439Glu
|
|
ENST00000509534.5:c.1338T>A
|
ENSP00000426858.1:p.Asp446Glu
|
|
ENST00000515008.1:n.652T>A
|
|
|
NM_001037633.1:c.1317T>A
|
NP_001032722.1:p.Asp439Glu
|
|
NM_022464.4:c.1317T>A
|
NP_071909.1:p.Asp439Glu
|
|
XM_011543570.1:c.1347T>A
|
XP_011541872.1:p.Asp449Glu
|
|
XM_011543570.2:c.1347T>A
|
XP_011541872.1:p.Asp449Glu
|
|
XM_024446164.1:c.1317T>A
|
XP_024301932.1:p.Asp439Glu
|
|
NM_022464.5:c.1317T>A
MANE Select
|
NP_071909.1:p.Asp439Glu
|
|
NM_001037633.2:c.1317T>A
|
NP_001032722.1:p.Asp439Glu
|
|