ENST00000298229.7:c.856C>T
MANE Select
|
ENSP00000298229.2:p.Leu286=
|
|
ENST00000298229.6:c.856C>T
|
ENSP00000298229.2:p.Leu286=
|
|
ENST00000538751.5:c.130C>T
|
ENSP00000444619.1:p.Leu44=
|
|
ENST00000540329.5:c.40C>T
|
ENSP00000440018.1:p.Leu14=
|
|
ENST00000541756.5:c.658C>T
|
ENSP00000446360.2:p.Leu220=
|
|
NM_001567.3:c.856C>T
|
NP_001558.3:p.Leu286=
|
|
XM_005273978.3:c.922C>T
|
XP_005274035.1:p.Leu308=
|
|
XM_005273979.3:c.922C>T
|
XP_005274036.1:p.Leu308=
|
|
XM_011544999.1:c.856C>T
|
XP_011543301.1:p.Leu286=
|
|
XM_011545000.1:c.922C>T
|
XP_011543302.1:p.Leu308=
|
|
XM_005273979.4:c.922C>T
|
XP_005274036.1:p.Leu308=
|
|
XM_011544999.2:c.856C>T
|
XP_011543301.1:p.Leu286=
|
|
XM_024448501.1:c.922C>T
|
XP_024304269.1:p.Leu308=
|
|
XM_024448502.1:c.922C>T
|
XP_024304270.1:p.Leu308=
|
|
XM_024448503.1:c.892C>T
|
XP_024304271.1:p.Leu298=
|
|
XM_024448504.1:c.856C>T
|
XP_024304272.1:p.Leu286=
|
|
XM_024448505.1:c.922C>T
|
XP_024304273.1:p.Leu308=
|
|
NM_001567.4:c.856C>T
MANE Select
|
NP_001558.3:p.Leu286=
|
|