ENST00000286657.10:c.1730A=
MANE Select
|
ENSP00000286657.4:p.Gln577=
|
|
ENST00000286657.8:c.1730A=
|
ENSP00000286657.4:p.Gln577=
|
|
ENST00000622135.1:c.1730A=
|
ENSP00000480055.1:p.Gln577=
|
|
NM_014243.2:c.1730A=
|
NP_055058.2:p.Gln577=
|
|
XM_011532421.1:c.1673A=
|
XP_011530723.1:p.Gln558=
|
|
XM_011532422.1:c.1646A=
|
XP_011530724.1:p.Gln549=
|
|
XM_011532423.1:c.1088A=
|
XP_011530725.1:p.Gln363=
|
|
XM_011532424.1:c.998A=
|
XP_011530726.1:p.Gln333=
|
|
XM_011532421.2:c.1673A=
|
XP_011530723.1:p.Gln558=
|
|
XM_011532422.3:c.1646A=
|
XP_011530724.1:p.Gln549=
|
|
NM_014243.3:c.1730A=
MANE Select
|
NP_055058.2:p.Gln577=
|
|