ENST00000317961.9:c.3586T>G
MANE Select
|
ENSP00000322408.4:p.Phe1196Val
|
|
ENST00000317961.8:c.3586T>G
|
ENSP00000322408.4:p.Phe1196Val
|
|
ENST00000382806.6:c.3415T>G
|
ENSP00000372256.2:p.Phe1139Val
|
|
ENST00000415360.1:c.502T>G
|
ENSP00000389433.1:p.Phe168Val
|
|
ENST00000440077.5:c.3463T>G
|
ENSP00000398543.1:p.Phe1155Val
|
|
ENST00000469599.6:n.2184T>G
|
|
|
ENST00000492117.1:n.3478T>G
|
|
|
ENST00000541639.5:c.3679T>G
|
ENSP00000444293.1:p.Phe1227Val
|
|
NM_001146705.1:c.3679T>G
|
NP_001140177.1:p.Phe1227Val
|
|
NM_001146706.1:c.3415T>G
|
NP_001140178.1:p.Phe1139Val
|
|
NM_004653.4:c.3586T>G
|
NP_004644.2:p.Phe1196Val
|
|
XM_005262560.1:c.3451T>G
|
XP_005262617.1:p.Phe1151Val
|
|
XM_005262561.1:c.3355T>G
|
XP_005262618.1:p.Phe1119Val
|
|
XM_011531468.1:c.3508T>G
|
XP_011529770.1:p.Phe1170Val
|
|
XR_244571.2:n.3874T>G
|
|
|
XR_430568.2:n.4208T>G
|
|
|
XM_005262560.3:c.3451T>G
|
XP_005262617.1:p.Phe1151Val
|
|
XM_005262561.3:c.3355T>G
|
XP_005262618.1:p.Phe1119Val
|
|
XM_011531468.3:c.3508T>G
|
XP_011529770.1:p.Phe1170Val
|
|
XM_024452495.1:c.1576T>G
|
XP_024308263.1:p.Phe526Val
|
|
XM_024452496.1:c.1342T>G
|
XP_024308264.1:p.Phe448Val
|
|
XR_001756009.2:n.4324T>G
|
|
|
XR_001756010.2:n.4324T>G
|
|
|
XR_001756011.2:n.4189T>G
|
|
|
XR_001756012.2:n.4337T>G
|
|
|
XR_001756013.2:n.3655T>G
|
|
|
XR_002958832.1:n.3756T>G
|
|
|
XR_002958834.1:n.3980T>G
|
|
|
XR_002958835.1:n.3863T>G
|
|
|
XR_002958836.1:n.4546T>G
|
|
|
XR_002958837.1:n.4353T>G
|
|
|
XR_244571.4:n.3873T>G
|
|
|
XR_430568.4:n.4207T>G
|
|
|
NM_001146706.2:c.3415T>G
|
NP_001140178.1:p.Phe1139Val
|
|
NM_004653.5:c.3586T>G
MANE Select
|
NP_004644.2:p.Phe1196Val
|
|
NM_001146705.2:c.3679T>G
|
NP_001140177.1:p.Phe1227Val
|
|