ENST00000366667.6:c.1344C>T
MANE Select
|
ENSP00000355627.5:p.Asn448=
|
|
ENST00000679738.1:c.1344C>T
|
ENSP00000505063.1:p.Asn448=
|
|
ENST00000679802.1:c.*803C>T
|
ENSP00000505184.1:n.*803C>T
|
|
ENST00000679854.1:n.5649C>T
|
|
|
ENST00000679957.1:c.1335C>T
|
ENSP00000506646.1:p.Asn445=
|
|
ENST00000680041.1:c.1344C>T
|
ENSP00000504866.1:p.Asn448=
|
|
ENST00000680783.1:c.829+6767C>T
|
ENSP00000506329.1:n.829+6767C>T
|
|
ENST00000681269.1:c.1344C>T
|
ENSP00000505985.1:p.Asn448=
|
|
ENST00000681347.1:n.3450C>T
|
|
|
ENST00000681514.1:c.1344C>T
|
ENSP00000505963.1:p.Asn448=
|
|
ENST00000681772.1:c.*838C>T
|
ENSP00000505829.1:n.*838C>T
|
|
ENST00000366667.4:c.1371C>T
|
ENSP00000355627.4:p.Asn457=
|
|
NM_000029.3:c.1371C>T
|
NP_000020.1:p.Asn457=
|
|
NM_000029.4:c.1371C>T
|
NP_000020.1:p.Asn457=
|
|
NM_001382817.3:c.1344C>T
|
NP_001369746.2:p.Asn448=
|
|
NM_001384479.1:c.1344C>T
MANE Select
|
NP_001371408.1:p.Asn448=
|
|