ENST00000362072.8:c.921C>T
MANE Select
|
ENSP00000354859.3:p.Leu307=
|
|
ENST00000346454.7:c.834C>T
|
ENSP00000278597.5:p.Leu278=
|
|
ENST00000362072.7:c.921C>T
|
ENSP00000354859.3:p.Leu307=
|
|
ENST00000538967.5:c.927C>T
|
ENSP00000438215.1:p.Leu309=
|
|
ENST00000542968.5:c.921C>T
|
ENSP00000442172.1:p.Leu307=
|
|
ENST00000544518.5:c.918C>T
|
ENSP00000441068.1:p.Leu306=
|
|
NM_000795.3:c.921C>T
|
NP_000786.1:p.Leu307=
|
|
NM_016574.3:c.834C>T
|
NP_057658.2:p.Leu278=
|
|
XM_017017296.2:c.921C>T
|
XP_016872785.1:p.Leu307=
|
|
NM_000795.4:c.921C>T
MANE Select
|
NP_000786.1:p.Leu307=
|
|
NM_016574.4:c.834C>T
|
NP_057658.2:p.Leu278=
|
|