ENST00000264670.11:c.768G>A
MANE Select
|
ENSP00000264670.6:p.Arg256=
|
|
ENST00000264670.10:c.768G>A
|
ENSP00000264670.6:p.Arg256=
|
|
ENST00000504374.5:c.*74G>A
|
ENSP00000421783.1:n.*74G>A
|
|
ENST00000505264.1:n.435G>A
|
|
|
ENST00000505892.5:n.1337G>A
|
|
|
ENST00000506139.5:c.663G>A
|
ENSP00000420957.1:p.Arg221=
|
|
NM_001193455.1:c.663G>A
|
NP_001180384.1:p.Arg221=
|
|
NM_017755.5:c.768G>A
|
NP_060225.4:p.Arg256=
|
|
NR_037947.1:n.1064G>A
|
|
|
NM_017755.6:c.768G>A
MANE Select
|
NP_060225.4:p.Arg256=
|
|
NM_001193455.2:c.663G>A
|
NP_001180384.1:p.Arg221=
|
|
NR_037947.2:n.748G>A
|
|
|