ENST00000317961.9:c.3338A>T
MANE Select
|
ENSP00000322408.4:p.Tyr1113Phe
|
|
ENST00000317961.8:c.3338A>T
|
ENSP00000322408.4:p.Tyr1113Phe
|
|
ENST00000382806.6:c.3167A>T
|
ENSP00000372256.2:p.Tyr1056Phe
|
|
ENST00000415360.1:c.254A>T
|
ENSP00000389433.1:p.Tyr85Phe
|
|
ENST00000440077.5:c.3215A>T
|
ENSP00000398543.1:p.Tyr1072Phe
|
|
ENST00000469599.6:n.1936A>T
|
|
|
ENST00000492117.1:n.3230A>T
|
|
|
ENST00000541639.5:c.3431A>T
|
ENSP00000444293.1:p.Tyr1144Phe
|
|
NM_001146705.1:c.3431A>T
|
NP_001140177.1:p.Tyr1144Phe
|
|
NM_001146706.1:c.3167A>T
|
NP_001140178.1:p.Tyr1056Phe
|
|
NM_004653.4:c.3338A>T
|
NP_004644.2:p.Tyr1113Phe
|
|
XM_005262560.1:c.3203A>T
|
XP_005262617.1:p.Tyr1068Phe
|
|
XM_005262561.1:c.3107A>T
|
XP_005262618.1:p.Tyr1036Phe
|
|
XM_011531468.1:c.3260A>T
|
XP_011529770.1:p.Tyr1087Phe
|
|
XR_244571.2:n.3626A>T
|
|
|
XR_430568.2:n.3960A>T
|
|
|
XM_005262560.3:c.3203A>T
|
XP_005262617.1:p.Tyr1068Phe
|
|
XM_005262561.3:c.3107A>T
|
XP_005262618.1:p.Tyr1036Phe
|
|
XM_011531468.3:c.3260A>T
|
XP_011529770.1:p.Tyr1087Phe
|
|
XM_024452495.1:c.1328A>T
|
XP_024308263.1:p.Tyr443Phe
|
|
XM_024452496.1:c.1094A>T
|
XP_024308264.1:p.Tyr365Phe
|
|
XR_001756009.2:n.4076A>T
|
|
|
XR_001756010.2:n.4076A>T
|
|
|
XR_001756011.2:n.3941A>T
|
|
|
XR_001756012.2:n.4089A>T
|
|
|
XR_001756013.2:n.3407A>T
|
|
|
XR_002958832.1:n.3508A>T
|
|
|
XR_002958834.1:n.3732A>T
|
|
|
XR_002958835.1:n.3615A>T
|
|
|
XR_002958836.1:n.4298A>T
|
|
|
XR_002958837.1:n.4105A>T
|
|
|
XR_244571.4:n.3625A>T
|
|
|
XR_430568.4:n.3959A>T
|
|
|
NM_001146706.2:c.3167A>T
|
NP_001140178.1:p.Tyr1056Phe
|
|
NM_004653.5:c.3338A>T
MANE Select
|
NP_004644.2:p.Tyr1113Phe
|
|
NM_001146705.2:c.3431A>T
|
NP_001140177.1:p.Tyr1144Phe
|
|