ENST00000370360.8:c.1191A>T
MANE Select
|
ENSP00000359385.3:p.Ser397=
|
|
ENST00000370360.7:c.1191A>T
|
ENSP00000359385.3:p.Ser397=
|
|
ENST00000463560.1:c.562+98A>T
|
|
|
ENST00000495106.5:c.1191A>T
|
ENSP00000436829.1:p.Ser397=
|
|
ENST00000495852.6:c.414A>T
|
ENSP00000469157.2:p.Ser138=
|
|
NM_053274.2:c.1191A>T
|
NP_444504.1:p.Ser397=
|
|
XM_005270400.1:c.1149A>T
|
XP_005270457.1:p.Ser383=
|
|
XM_005270401.2:c.1065A>T
|
XP_005270458.1:p.Ser355=
|
|
XM_006710309.1:c.690A>T
|
XP_006710372.1:p.Ser230=
|
|
XM_011540544.1:c.1191A>T
|
XP_011538846.1:p.Ser397=
|
|
XM_011540545.1:c.1191A>T
|
XP_011538847.1:p.Ser397=
|
|
XM_011540546.1:c.1191A>T
|
XP_011538848.1:p.Ser397=
|
|
XR_946529.1:n.1309+98A>T
|
|
|
NM_001319683.1:c.1149A>T
|
NP_001306612.1:p.Ser383=
|
|
NR_135089.1:n.1306A>T
|
|
|
XM_005270401.3:c.1065A>T
|
XP_005270458.1:p.Ser355=
|
|
XM_006710309.2:c.690A>T
|
XP_006710372.1:p.Ser230=
|
|
XM_011540546.2:c.1191A>T
|
XP_011538848.1:p.Ser397=
|
|
XM_017000137.1:c.1290A>T
|
XP_016855626.1:p.Ser430=
|
|
XM_017000138.1:c.1248A>T
|
XP_016855627.1:p.Ser416=
|
|
XM_017000139.1:c.1293+98A>T
|
XP_016855628.1:n.1293+98A>T
|
|
XM_017000140.1:c.1164A>T
|
XP_016855629.1:p.Ser388=
|
|
XM_017000141.1:c.1194+98A>T
|
XP_016855630.1:n.1194+98A>T
|
|
XM_017000142.1:c.648A>T
|
XP_016855631.1:p.Ser216=
|
|
XM_017000143.1:c.648A>T
|
XP_016855632.1:p.Ser216=
|
|
XM_017000144.1:c.420A>T
|
XP_016855633.1:p.Ser140=
|
|
XR_002959248.1:n.1677+98A>T
|
|
|
XR_002959249.1:n.1309+98A>T
|
|
|
NM_053274.3:c.1191A>T
MANE Select
|
NP_444504.1:p.Ser397=
|
|
NM_001319683.2:c.1149A>T
|
NP_001306612.1:p.Ser383=
|
|
NR_135089.2:n.1284A>T
|
|
|