ENST00000317961.9:c.3337T>A
MANE Select
|
ENSP00000322408.4:p.Tyr1113Asn
|
|
ENST00000317961.8:c.3337T>A
|
ENSP00000322408.4:p.Tyr1113Asn
|
|
ENST00000382806.6:c.3166T>A
|
ENSP00000372256.2:p.Tyr1056Asn
|
|
ENST00000415360.1:c.253T>A
|
ENSP00000389433.1:p.Tyr85Asn
|
|
ENST00000440077.5:c.3214T>A
|
ENSP00000398543.1:p.Tyr1072Asn
|
|
ENST00000469599.6:n.1935T>A
|
|
|
ENST00000492117.1:n.3229T>A
|
|
|
ENST00000541639.5:c.3430T>A
|
ENSP00000444293.1:p.Tyr1144Asn
|
|
NM_001146705.1:c.3430T>A
|
NP_001140177.1:p.Tyr1144Asn
|
|
NM_001146706.1:c.3166T>A
|
NP_001140178.1:p.Tyr1056Asn
|
|
NM_004653.4:c.3337T>A
|
NP_004644.2:p.Tyr1113Asn
|
|
XM_005262560.1:c.3202T>A
|
XP_005262617.1:p.Tyr1068Asn
|
|
XM_005262561.1:c.3106T>A
|
XP_005262618.1:p.Tyr1036Asn
|
|
XM_011531468.1:c.3259T>A
|
XP_011529770.1:p.Tyr1087Asn
|
|
XR_244571.2:n.3625T>A
|
|
|
XR_430568.2:n.3959T>A
|
|
|
XM_005262560.3:c.3202T>A
|
XP_005262617.1:p.Tyr1068Asn
|
|
XM_005262561.3:c.3106T>A
|
XP_005262618.1:p.Tyr1036Asn
|
|
XM_011531468.3:c.3259T>A
|
XP_011529770.1:p.Tyr1087Asn
|
|
XM_024452495.1:c.1327T>A
|
XP_024308263.1:p.Tyr443Asn
|
|
XM_024452496.1:c.1093T>A
|
XP_024308264.1:p.Tyr365Asn
|
|
XR_001756009.2:n.4075T>A
|
|
|
XR_001756010.2:n.4075T>A
|
|
|
XR_001756011.2:n.3940T>A
|
|
|
XR_001756012.2:n.4088T>A
|
|
|
XR_001756013.2:n.3406T>A
|
|
|
XR_002958832.1:n.3507T>A
|
|
|
XR_002958834.1:n.3731T>A
|
|
|
XR_002958835.1:n.3614T>A
|
|
|
XR_002958836.1:n.4297T>A
|
|
|
XR_002958837.1:n.4104T>A
|
|
|
XR_244571.4:n.3624T>A
|
|
|
XR_430568.4:n.3958T>A
|
|
|
NM_001146706.2:c.3166T>A
|
NP_001140178.1:p.Tyr1056Asn
|
|
NM_004653.5:c.3337T>A
MANE Select
|
NP_004644.2:p.Tyr1113Asn
|
|
NM_001146705.2:c.3430T>A
|
NP_001140177.1:p.Tyr1144Asn
|
|