ENST00000310638.9:c.1308T>G
MANE Select
|
ENSP00000311095.4:p.Phe436Leu
|
|
ENST00000310638.8:c.1308T>G
|
ENSP00000311095.4:p.Phe436Leu
|
|
ENST00000371904.8:c.1311T>G
|
ENSP00000360971.4:p.Phe437Leu
|
|
ENST00000371905.1:c.1308T>G
|
ENSP00000360972.1:p.Phe436Leu
|
|
ENST00000462347.5:c.1014T>G
|
ENSP00000477495.1:p.Phe338Leu
|
|
ENST00000465874.5:c.*106T>G
|
ENSP00000476368.1:n.*106T>G
|
|
ENST00000468629.5:c.*13T>G
|
ENSP00000476619.1:n.*13T>G
|
|
ENST00000474458.5:c.*13T>G
|
ENSP00000476988.1:n.*13T>G
|
|
ENST00000475477.5:c.*102T>G
|
ENSP00000476854.1:n.*102T>G
|
|
NM_000778.3:c.1308T>G
|
NP_000769.2:p.Phe436Leu
|
|
XM_005270539.1:c.1014T>G
|
XP_005270596.1:p.Phe338Leu
|
|
XM_011540826.1:c.1326T>G
|
XP_011539128.1:p.Phe442Leu
|
|
XM_011540827.1:c.1032T>G
|
XP_011539129.1:p.Phe344Leu
|
|
XM_011540828.1:c.1014T>G
|
XP_011539130.1:p.Phe338Leu
|
|
XR_246241.1:n.1212T>G
|
|
|
XR_246242.1:n.1196T>G
|
|
|
NM_001319155.1:c.1212T>G
|
NP_001306084.1:p.Phe404Leu
|
|
NM_001363587.1:c.1014T>G
|
NP_001350516.1:p.Phe338Leu
|
|
NR_134988.1:n.1013T>G
|
|
|
NR_134989.1:n.1204T>G
|
|
|
NR_134990.1:n.1198T>G
|
|
|
NR_134991.1:n.1185T>G
|
|
|
NR_134992.1:n.814T>G
|
|
|
NR_134993.1:n.948T>G
|
|
|
NR_134994.1:n.1220T>G
|
|
|
XM_017000465.1:c.996T>G
|
XP_016855954.1:p.Phe332Leu
|
|
XR_001737005.1:n.1286T>G
|
|
|
NM_000778.4:c.1308T>G
MANE Select
|
NP_000769.2:p.Phe436Leu
|
|
NM_001319155.2:c.1212T>G
|
NP_001306084.1:p.Phe404Leu
|
|
NM_001363587.2:c.1014T>G
|
NP_001350516.1:p.Phe338Leu
|
|
NR_134988.2:n.1005T>G
|
|
|
NR_134989.2:n.1196T>G
|
|
|
NR_134990.2:n.1190T>G
|
|
|
NR_134991.2:n.1177T>G
|
|
|
NR_134992.2:n.806T>G
|
|
|
NR_134993.2:n.940T>G
|
|
|
NR_134994.2:n.1212T>G
|
|
|