ENST00000264670.11:c.756T>A
MANE Select
|
ENSP00000264670.6:p.Asp252Glu
|
|
ENST00000264670.10:c.756T>A
|
ENSP00000264670.6:p.Asp252Glu
|
|
ENST00000504374.5:c.*62T>A
|
ENSP00000421783.1:n.*62T>A
|
|
ENST00000505264.1:n.423T>A
|
|
|
ENST00000505892.5:n.1325T>A
|
|
|
ENST00000506139.5:c.651T>A
|
ENSP00000420957.1:p.Asp217Glu
|
|
NM_001193455.1:c.651T>A
|
NP_001180384.1:p.Asp217Glu
|
|
NM_017755.5:c.756T>A
|
NP_060225.4:p.Asp252Glu
|
|
NR_037947.1:n.1052T>A
|
|
|
NM_017755.6:c.756T>A
MANE Select
|
NP_060225.4:p.Asp252Glu
|
|
NM_001193455.2:c.651T>A
|
NP_001180384.1:p.Asp217Glu
|
|
NR_037947.2:n.736T>A
|
|
|