ENST00000695651.1:n.2257C=
|
|
|
ENST00000695653.1:c.1818C=
|
ENSP00000512084.1:p.Arg606=
|
|
ENST00000695654.1:c.2934C=
|
ENSP00000512085.1:p.Arg978=
|
|
ENST00000695690.1:n.100C=
|
|
|
ENST00000695691.1:n.100C=
|
|
|
ENST00000245907.11:c.3909C=
MANE Select
|
ENSP00000245907.4:p.Arg1303=
|
|
ENST00000245907.10:c.3909C=
|
ENSP00000245907.4:p.Arg1303=
|
|
ENST00000596238.1:n.352C=
|
|
|
ENST00000601008.1:c.241+1698C=
|
ENSP00000471384.1:n.241+1698C=
|
|
NM_000064.3:c.3909C=
|
NP_000055.2:p.Arg1303=
|
|
NM_000064.4:c.3909C=
MANE Select
|
NP_000055.2:p.Arg1303=
|
|