ENST00000310638.9:c.1306T>C
MANE Select
|
ENSP00000311095.4:p.Phe436Leu
|
|
ENST00000310638.8:c.1306T>C
|
ENSP00000311095.4:p.Phe436Leu
|
|
ENST00000371904.8:c.1309T>C
|
ENSP00000360971.4:p.Phe437Leu
|
|
ENST00000371905.1:c.1306T>C
|
ENSP00000360972.1:p.Phe436Leu
|
|
ENST00000462347.5:c.1012T>C
|
ENSP00000477495.1:p.Phe338Leu
|
|
ENST00000465874.5:c.*104T>C
|
ENSP00000476368.1:n.*104T>C
|
|
ENST00000468629.5:c.*11T>C
|
ENSP00000476619.1:n.*11T>C
|
|
ENST00000474458.5:c.*11T>C
|
ENSP00000476988.1:n.*11T>C
|
|
ENST00000475477.5:c.*100T>C
|
ENSP00000476854.1:n.*100T>C
|
|
NM_000778.3:c.1306T>C
|
NP_000769.2:p.Phe436Leu
|
|
XM_005270539.1:c.1012T>C
|
XP_005270596.1:p.Phe338Leu
|
|
XM_011540826.1:c.1324T>C
|
XP_011539128.1:p.Phe442Leu
|
|
XM_011540827.1:c.1030T>C
|
XP_011539129.1:p.Phe344Leu
|
|
XM_011540828.1:c.1012T>C
|
XP_011539130.1:p.Phe338Leu
|
|
XR_246241.1:n.1210T>C
|
|
|
XR_246242.1:n.1194T>C
|
|
|
NM_001319155.1:c.1210T>C
|
NP_001306084.1:p.Phe404Leu
|
|
NM_001363587.1:c.1012T>C
|
NP_001350516.1:p.Phe338Leu
|
|
NR_134988.1:n.1011T>C
|
|
|
NR_134989.1:n.1202T>C
|
|
|
NR_134990.1:n.1196T>C
|
|
|
NR_134991.1:n.1183T>C
|
|
|
NR_134992.1:n.812T>C
|
|
|
NR_134993.1:n.946T>C
|
|
|
NR_134994.1:n.1218T>C
|
|
|
XM_017000465.1:c.994T>C
|
XP_016855954.1:p.Phe332Leu
|
|
XR_001737005.1:n.1284T>C
|
|
|
NM_000778.4:c.1306T>C
MANE Select
|
NP_000769.2:p.Phe436Leu
|
|
NM_001319155.2:c.1210T>C
|
NP_001306084.1:p.Phe404Leu
|
|
NM_001363587.2:c.1012T>C
|
NP_001350516.1:p.Phe338Leu
|
|
NR_134988.2:n.1003T>C
|
|
|
NR_134989.2:n.1194T>C
|
|
|
NR_134990.2:n.1188T>C
|
|
|
NR_134991.2:n.1175T>C
|
|
|
NR_134992.2:n.804T>C
|
|
|
NR_134993.2:n.938T>C
|
|
|
NR_134994.2:n.1210T>C
|
|
|