ENST00000317961.9:c.3337T>G
MANE Select
|
ENSP00000322408.4:p.Tyr1113Asp
|
|
ENST00000317961.8:c.3337T>G
|
ENSP00000322408.4:p.Tyr1113Asp
|
|
ENST00000382806.6:c.3166T>G
|
ENSP00000372256.2:p.Tyr1056Asp
|
|
ENST00000415360.1:c.253T>G
|
ENSP00000389433.1:p.Tyr85Asp
|
|
ENST00000440077.5:c.3214T>G
|
ENSP00000398543.1:p.Tyr1072Asp
|
|
ENST00000469599.6:n.1935T>G
|
|
|
ENST00000492117.1:n.3229T>G
|
|
|
ENST00000541639.5:c.3430T>G
|
ENSP00000444293.1:p.Tyr1144Asp
|
|
NM_001146705.1:c.3430T>G
|
NP_001140177.1:p.Tyr1144Asp
|
|
NM_001146706.1:c.3166T>G
|
NP_001140178.1:p.Tyr1056Asp
|
|
NM_004653.4:c.3337T>G
|
NP_004644.2:p.Tyr1113Asp
|
|
XM_005262560.1:c.3202T>G
|
XP_005262617.1:p.Tyr1068Asp
|
|
XM_005262561.1:c.3106T>G
|
XP_005262618.1:p.Tyr1036Asp
|
|
XM_011531468.1:c.3259T>G
|
XP_011529770.1:p.Tyr1087Asp
|
|
XR_244571.2:n.3625T>G
|
|
|
XR_430568.2:n.3959T>G
|
|
|
XM_005262560.3:c.3202T>G
|
XP_005262617.1:p.Tyr1068Asp
|
|
XM_005262561.3:c.3106T>G
|
XP_005262618.1:p.Tyr1036Asp
|
|
XM_011531468.3:c.3259T>G
|
XP_011529770.1:p.Tyr1087Asp
|
|
XM_024452495.1:c.1327T>G
|
XP_024308263.1:p.Tyr443Asp
|
|
XM_024452496.1:c.1093T>G
|
XP_024308264.1:p.Tyr365Asp
|
|
XR_001756009.2:n.4075T>G
|
|
|
XR_001756010.2:n.4075T>G
|
|
|
XR_001756011.2:n.3940T>G
|
|
|
XR_001756012.2:n.4088T>G
|
|
|
XR_001756013.2:n.3406T>G
|
|
|
XR_002958832.1:n.3507T>G
|
|
|
XR_002958834.1:n.3731T>G
|
|
|
XR_002958835.1:n.3614T>G
|
|
|
XR_002958836.1:n.4297T>G
|
|
|
XR_002958837.1:n.4104T>G
|
|
|
XR_244571.4:n.3624T>G
|
|
|
XR_430568.4:n.3958T>G
|
|
|
NM_001146706.2:c.3166T>G
|
NP_001140178.1:p.Tyr1056Asp
|
|
NM_004653.5:c.3337T>G
MANE Select
|
NP_004644.2:p.Tyr1113Asp
|
|
NM_001146705.2:c.3430T>G
|
NP_001140177.1:p.Tyr1144Asp
|
|