ENST00000339818.9:c.363G>T
MANE Select
|
ENSP00000344566.4:p.Leu121=
|
|
ENST00000325223.7:c.363G>T
|
ENSP00000317302.7:p.Leu121=
|
|
ENST00000339818.8:c.363G>T
|
ENSP00000344566.4:p.Leu121=
|
|
ENST00000397956.7:c.363G>T
|
ENSP00000381047.3:p.Leu121=
|
|
ENST00000462742.1:n.2534G>T
|
|
|
ENST00000478674.1:n.422G>T
|
|
|
ENST00000496321.5:n.479G>T
|
|
|
NM_001271440.1:c.363G>T
|
NP_001258369.1:p.Leu121=
|
|
NM_001271441.1:c.363G>T
|
NP_001258370.1:p.Leu121=
|
|
NM_001271442.1:c.240G>T
|
NP_001258371.1:p.Leu80=
|
|
NM_004928.2:c.363G>T
|
NP_004919.1:p.Leu121=
|
|
XM_006724051.2:c.438G>T
|
XP_006724114.1:p.Leu146=
|
|
XM_006724052.2:c.438G>T
|
XP_006724115.1:p.Leu146=
|
|
XM_006724053.2:c.39G>T
|
XP_006724116.1:p.Leu13=
|
|
XR_937571.1:n.566G>T
|
|
|
XM_006724051.3:c.438G>T
|
XP_006724114.1:p.Leu146=
|
|
XM_006724053.3:c.39G>T
|
XP_006724116.1:p.Leu13=
|
|
XM_017028470.1:c.567G>T
|
XP_016883959.1:p.Leu189=
|
|
XM_017028471.1:c.312G>T
|
XP_016883960.1:p.Leu104=
|
|
XM_017028472.1:c.39G>T
|
XP_016883961.1:p.Leu13=
|
|
XR_937571.2:n.573G>T
|
|
|
NM_004928.3:c.363G>T
MANE Select
|
NP_004919.1:p.Leu121=
|
|
NM_001271440.2:c.363G>T
|
NP_001258369.1:p.Leu121=
|
|
NM_001271441.2:c.363G>T
|
NP_001258370.1:p.Leu121=
|
|