ENST00000317961.9:c.3660A>T
MANE Select
|
ENSP00000322408.4:p.Leu1220=
|
|
ENST00000317961.8:c.3660A>T
|
ENSP00000322408.4:p.Leu1220=
|
|
ENST00000382806.6:c.3489A>T
|
ENSP00000372256.2:p.Leu1163=
|
|
ENST00000415360.1:c.576A>T
|
ENSP00000389433.1:p.Leu192=
|
|
ENST00000440077.5:c.3537A>T
|
ENSP00000398543.1:p.Leu1179=
|
|
ENST00000469599.6:n.2258A>T
|
|
|
ENST00000492117.1:n.3552A>T
|
|
|
ENST00000541639.5:c.3753A>T
|
ENSP00000444293.1:p.Leu1251=
|
|
NM_001146705.1:c.3753A>T
|
NP_001140177.1:p.Leu1251=
|
|
NM_001146706.1:c.3489A>T
|
NP_001140178.1:p.Leu1163=
|
|
NM_004653.4:c.3660A>T
|
NP_004644.2:p.Leu1220=
|
|
XM_005262560.1:c.3525A>T
|
XP_005262617.1:p.Leu1175=
|
|
XM_005262561.1:c.3429A>T
|
XP_005262618.1:p.Leu1143=
|
|
XM_011531468.1:c.3582A>T
|
XP_011529770.1:p.Leu1194=
|
|
XR_244571.2:n.3948A>T
|
|
|
XR_430568.2:n.4282A>T
|
|
|
XM_005262560.3:c.3525A>T
|
XP_005262617.1:p.Leu1175=
|
|
XM_005262561.3:c.3429A>T
|
XP_005262618.1:p.Leu1143=
|
|
XM_011531468.3:c.3582A>T
|
XP_011529770.1:p.Leu1194=
|
|
XM_024452495.1:c.1650A>T
|
XP_024308263.1:p.Leu550=
|
|
XM_024452496.1:c.1416A>T
|
XP_024308264.1:p.Leu472=
|
|
XR_001756009.2:n.4398A>T
|
|
|
XR_001756010.2:n.4398A>T
|
|
|
XR_001756011.2:n.4263A>T
|
|
|
XR_001756012.2:n.4411A>T
|
|
|
XR_001756013.2:n.3729A>T
|
|
|
XR_002958832.1:n.3830A>T
|
|
|
XR_002958834.1:n.4054A>T
|
|
|
XR_002958835.1:n.3937A>T
|
|
|
XR_002958836.1:n.4620A>T
|
|
|
XR_002958837.1:n.4427A>T
|
|
|
XR_244571.4:n.3947A>T
|
|
|
XR_430568.4:n.4281A>T
|
|
|
NM_001146706.2:c.3489A>T
|
NP_001140178.1:p.Leu1163=
|
|
NM_004653.5:c.3660A>T
MANE Select
|
NP_004644.2:p.Leu1220=
|
|
NM_001146705.2:c.3753A>T
|
NP_001140177.1:p.Leu1251=
|
|