ENST00000370360.8:c.1183T>G
MANE Select
|
ENSP00000359385.3:p.Leu395Val
|
|
ENST00000370360.7:c.1183T>G
|
ENSP00000359385.3:p.Leu395Val
|
|
ENST00000463560.1:c.562+90T>G
|
|
|
ENST00000495106.5:c.1183T>G
|
ENSP00000436829.1:p.Leu395Val
|
|
ENST00000495852.6:c.406T>G
|
ENSP00000469157.2:p.Leu136Val
|
|
NM_053274.2:c.1183T>G
|
NP_444504.1:p.Leu395Val
|
|
XM_005270400.1:c.1141T>G
|
XP_005270457.1:p.Leu381Val
|
|
XM_005270401.2:c.1057T>G
|
XP_005270458.1:p.Leu353Val
|
|
XM_006710309.1:c.682T>G
|
XP_006710372.1:p.Leu228Val
|
|
XM_011540544.1:c.1183T>G
|
XP_011538846.1:p.Leu395Val
|
|
XM_011540545.1:c.1183T>G
|
XP_011538847.1:p.Leu395Val
|
|
XM_011540546.1:c.1183T>G
|
XP_011538848.1:p.Leu395Val
|
|
XR_946529.1:n.1309+90T>G
|
|
|
NM_001319683.1:c.1141T>G
|
NP_001306612.1:p.Leu381Val
|
|
NR_135089.1:n.1298T>G
|
|
|
XM_005270401.3:c.1057T>G
|
XP_005270458.1:p.Leu353Val
|
|
XM_006710309.2:c.682T>G
|
XP_006710372.1:p.Leu228Val
|
|
XM_011540546.2:c.1183T>G
|
XP_011538848.1:p.Leu395Val
|
|
XM_017000137.1:c.1282T>G
|
XP_016855626.1:p.Leu428Val
|
|
XM_017000138.1:c.1240T>G
|
XP_016855627.1:p.Leu414Val
|
|
XM_017000139.1:c.1293+90T>G
|
XP_016855628.1:n.1293+90T>G
|
|
XM_017000140.1:c.1156T>G
|
XP_016855629.1:p.Leu386Val
|
|
XM_017000141.1:c.1194+90T>G
|
XP_016855630.1:n.1194+90T>G
|
|
XM_017000142.1:c.640T>G
|
XP_016855631.1:p.Leu214Val
|
|
XM_017000143.1:c.640T>G
|
XP_016855632.1:p.Leu214Val
|
|
XM_017000144.1:c.412T>G
|
XP_016855633.1:p.Leu138Val
|
|
XR_002959248.1:n.1677+90T>G
|
|
|
XR_002959249.1:n.1309+90T>G
|
|
|
NM_053274.3:c.1183T>G
MANE Select
|
NP_444504.1:p.Leu395Val
|
|
NM_001319683.2:c.1141T>G
|
NP_001306612.1:p.Leu381Val
|
|
NR_135089.2:n.1276T>G
|
|
|