ENST00000317961.9:c.3463A>T
MANE Select
|
ENSP00000322408.4:p.Asn1155Tyr
|
|
ENST00000317961.8:c.3463A>T
|
ENSP00000322408.4:p.Asn1155Tyr
|
|
ENST00000382806.6:c.3292A>T
|
ENSP00000372256.2:p.Asn1098Tyr
|
|
ENST00000415360.1:c.379A>T
|
ENSP00000389433.1:p.Asn127Tyr
|
|
ENST00000440077.5:c.3340A>T
|
ENSP00000398543.1:p.Asn1114Tyr
|
|
ENST00000469599.6:n.2061A>T
|
|
|
ENST00000492117.1:n.3355A>T
|
|
|
ENST00000541639.5:c.3556A>T
|
ENSP00000444293.1:p.Asn1186Tyr
|
|
NM_001146705.1:c.3556A>T
|
NP_001140177.1:p.Asn1186Tyr
|
|
NM_001146706.1:c.3292A>T
|
NP_001140178.1:p.Asn1098Tyr
|
|
NM_004653.4:c.3463A>T
|
NP_004644.2:p.Asn1155Tyr
|
|
XM_005262560.1:c.3328A>T
|
XP_005262617.1:p.Asn1110Tyr
|
|
XM_005262561.1:c.3232A>T
|
XP_005262618.1:p.Asn1078Tyr
|
|
XM_011531468.1:c.3385A>T
|
XP_011529770.1:p.Asn1129Tyr
|
|
XR_244571.2:n.3751A>T
|
|
|
XR_430568.2:n.4085A>T
|
|
|
XM_005262560.3:c.3328A>T
|
XP_005262617.1:p.Asn1110Tyr
|
|
XM_005262561.3:c.3232A>T
|
XP_005262618.1:p.Asn1078Tyr
|
|
XM_011531468.3:c.3385A>T
|
XP_011529770.1:p.Asn1129Tyr
|
|
XM_024452495.1:c.1453A>T
|
XP_024308263.1:p.Asn485Tyr
|
|
XM_024452496.1:c.1219A>T
|
XP_024308264.1:p.Asn407Tyr
|
|
XR_001756009.2:n.4201A>T
|
|
|
XR_001756010.2:n.4201A>T
|
|
|
XR_001756011.2:n.4066A>T
|
|
|
XR_001756012.2:n.4214A>T
|
|
|
XR_001756013.2:n.3532A>T
|
|
|
XR_002958832.1:n.3633A>T
|
|
|
XR_002958834.1:n.3857A>T
|
|
|
XR_002958835.1:n.3740A>T
|
|
|
XR_002958836.1:n.4423A>T
|
|
|
XR_002958837.1:n.4230A>T
|
|
|
XR_244571.4:n.3750A>T
|
|
|
XR_430568.4:n.4084A>T
|
|
|
NM_001146706.2:c.3292A>T
|
NP_001140178.1:p.Asn1098Tyr
|
|
NM_004653.5:c.3463A>T
MANE Select
|
NP_004644.2:p.Asn1155Tyr
|
|
NM_001146705.2:c.3556A>T
|
NP_001140177.1:p.Asn1186Tyr
|
|