ENST00000317961.9:c.3650C>A
MANE Select
|
ENSP00000322408.4:p.Ser1217Tyr
|
|
ENST00000317961.8:c.3650C>A
|
ENSP00000322408.4:p.Ser1217Tyr
|
|
ENST00000382806.6:c.3479C>A
|
ENSP00000372256.2:p.Ser1160Tyr
|
|
ENST00000415360.1:c.566C>A
|
ENSP00000389433.1:p.Ser189Tyr
|
|
ENST00000440077.5:c.3527C>A
|
ENSP00000398543.1:p.Ser1176Tyr
|
|
ENST00000469599.6:n.2248C>A
|
|
|
ENST00000492117.1:n.3542C>A
|
|
|
ENST00000541639.5:c.3743C>A
|
ENSP00000444293.1:p.Ser1248Tyr
|
|
NM_001146705.1:c.3743C>A
|
NP_001140177.1:p.Ser1248Tyr
|
|
NM_001146706.1:c.3479C>A
|
NP_001140178.1:p.Ser1160Tyr
|
|
NM_004653.4:c.3650C>A
|
NP_004644.2:p.Ser1217Tyr
|
|
XM_005262560.1:c.3515C>A
|
XP_005262617.1:p.Ser1172Tyr
|
|
XM_005262561.1:c.3419C>A
|
XP_005262618.1:p.Ser1140Tyr
|
|
XM_011531468.1:c.3572C>A
|
XP_011529770.1:p.Ser1191Tyr
|
|
XR_244571.2:n.3938C>A
|
|
|
XR_430568.2:n.4272C>A
|
|
|
XM_005262560.3:c.3515C>A
|
XP_005262617.1:p.Ser1172Tyr
|
|
XM_005262561.3:c.3419C>A
|
XP_005262618.1:p.Ser1140Tyr
|
|
XM_011531468.3:c.3572C>A
|
XP_011529770.1:p.Ser1191Tyr
|
|
XM_024452495.1:c.1640C>A
|
XP_024308263.1:p.Ser547Tyr
|
|
XM_024452496.1:c.1406C>A
|
XP_024308264.1:p.Ser469Tyr
|
|
XR_001756009.2:n.4388C>A
|
|
|
XR_001756010.2:n.4388C>A
|
|
|
XR_001756011.2:n.4253C>A
|
|
|
XR_001756012.2:n.4401C>A
|
|
|
XR_001756013.2:n.3719C>A
|
|
|
XR_002958832.1:n.3820C>A
|
|
|
XR_002958834.1:n.4044C>A
|
|
|
XR_002958835.1:n.3927C>A
|
|
|
XR_002958836.1:n.4610C>A
|
|
|
XR_002958837.1:n.4417C>A
|
|
|
XR_244571.4:n.3937C>A
|
|
|
XR_430568.4:n.4271C>A
|
|
|
NM_001146706.2:c.3479C>A
|
NP_001140178.1:p.Ser1160Tyr
|
|
NM_004653.5:c.3650C>A
MANE Select
|
NP_004644.2:p.Ser1217Tyr
|
|
NM_001146705.2:c.3743C>A
|
NP_001140177.1:p.Ser1248Tyr
|
|