ENST00000370360.8:c.1202A>G
MANE Select
|
ENSP00000359385.3:p.Tyr401Cys
|
|
ENST00000370360.7:c.1202A>G
|
ENSP00000359385.3:p.Tyr401Cys
|
|
ENST00000463560.1:c.562+109A>G
|
|
|
ENST00000495106.5:c.1202A>G
|
ENSP00000436829.1:p.Tyr401Cys
|
|
ENST00000495852.6:c.425A>G
|
ENSP00000469157.2:p.Tyr142Cys
|
|
NM_053274.2:c.1202A>G
|
NP_444504.1:p.Tyr401Cys
|
|
XM_005270400.1:c.1160A>G
|
XP_005270457.1:p.Tyr387Cys
|
|
XM_005270401.2:c.1076A>G
|
XP_005270458.1:p.Tyr359Cys
|
|
XM_006710309.1:c.701A>G
|
XP_006710372.1:p.Tyr234Cys
|
|
XM_011540544.1:c.1202A>G
|
XP_011538846.1:p.Tyr401Cys
|
|
XM_011540545.1:c.1202A>G
|
XP_011538847.1:p.Tyr401Cys
|
|
XM_011540546.1:c.1202A>G
|
XP_011538848.1:p.Tyr401Cys
|
|
XR_946529.1:n.1309+109A>G
|
|
|
NM_001319683.1:c.1160A>G
|
NP_001306612.1:p.Tyr387Cys
|
|
NR_135089.1:n.1317A>G
|
|
|
XM_005270401.3:c.1076A>G
|
XP_005270458.1:p.Tyr359Cys
|
|
XM_006710309.2:c.701A>G
|
XP_006710372.1:p.Tyr234Cys
|
|
XM_011540546.2:c.1202A>G
|
XP_011538848.1:p.Tyr401Cys
|
|
XM_017000137.1:c.1301A>G
|
XP_016855626.1:p.Tyr434Cys
|
|
XM_017000138.1:c.1259A>G
|
XP_016855627.1:p.Tyr420Cys
|
|
XM_017000139.1:c.1293+109A>G
|
XP_016855628.1:n.1293+109A>G
|
|
XM_017000140.1:c.1175A>G
|
XP_016855629.1:p.Tyr392Cys
|
|
XM_017000141.1:c.1194+109A>G
|
XP_016855630.1:n.1194+109A>G
|
|
XM_017000142.1:c.659A>G
|
XP_016855631.1:p.Tyr220Cys
|
|
XM_017000143.1:c.659A>G
|
XP_016855632.1:p.Tyr220Cys
|
|
XM_017000144.1:c.431A>G
|
XP_016855633.1:p.Tyr144Cys
|
|
XR_002959248.1:n.1677+109A>G
|
|
|
XR_002959249.1:n.1309+109A>G
|
|
|
NM_053274.3:c.1202A>G
MANE Select
|
NP_444504.1:p.Tyr401Cys
|
|
NM_001319683.2:c.1160A>G
|
NP_001306612.1:p.Tyr387Cys
|
|
NR_135089.2:n.1295A>G
|
|
|