|
ENST00000375687.10:c.3845T>A
MANE Select
|
ENSP00000364839.4:p.Phe1282Tyr
|
|
|
ENST00000646985.1:c.3662T>A
|
ENSP00000495053.1:p.Phe1221Tyr
|
|
|
ENST00000647223.1:n.6198T>A
|
|
|
|
ENST00000651418.1:c.1870-1873T>A
|
ENSP00000499150.1:n.1870-1873T>A
|
|
|
ENST00000306058.9:c.3830T>A
|
ENSP00000305119.5:p.Phe1277Tyr
|
|
|
ENST00000375687.8:c.3845T>A
|
ENSP00000364839.4:p.Phe1282Tyr
|
|
|
ENST00000613218.4:c.3845T>A
|
ENSP00000480487.1:p.Phe1282Tyr
|
|
|
ENST00000620121.4:c.3845T>A
|
ENSP00000481978.1:p.Phe1282Tyr
|
|
|
NM_015338.5:c.3845T>A , LRG_630t1:c.3845T>A
|
NP_056153.2:p.Phe1282Tyr
|
|
|
XM_006723727.2:c.3842T>A
|
XP_006723790.1:p.Phe1281Tyr
|
|
|
XM_006723728.2:c.3815T>A
|
XP_006723791.1:p.Phe1272Tyr
|
|
|
XM_006723730.2:c.3761T>A
|
XP_006723793.1:p.Phe1254Tyr
|
|
|
XM_006723732.2:c.3662T>A
|
XP_006723795.1:p.Phe1221Tyr
|
|
|
XM_006723733.1:c.3161T>A
|
XP_006723796.1:p.Phe1054Tyr
|
|
|
XM_011528647.1:c.4109T>A
|
XP_011526949.1:p.Phe1370Tyr
|
|
|
XM_011528648.1:c.4106T>A
|
XP_011526950.1:p.Phe1369Tyr
|
|
|
XM_011528649.1:c.4025T>A
|
XP_011526951.1:p.Phe1342Tyr
|
|
|
XM_011528650.1:c.3956T>A
|
XP_011526952.1:p.Phe1319Tyr
|
|
|
XM_011528651.1:c.3824T>A
|
XP_011526953.1:p.Phe1275Tyr
|
|
|
XM_011528652.1:c.3761T>A
|
XP_011526954.1:p.Phe1254Tyr
|
|
|
NM_001363734.1:c.3662T>A
|
NP_001350663.1:p.Phe1221Tyr
|
|
|
XM_006723727.3:c.3842T>A
|
XP_006723790.1:p.Phe1281Tyr
|
|
|
XM_006723728.3:c.3815T>A
|
XP_006723791.1:p.Phe1272Tyr
|
|
|
XM_006723730.4:c.3761T>A
|
XP_006723793.1:p.Phe1254Tyr
|
|
|
XM_011528648.3:c.4106T>A
|
XP_011526950.1:p.Phe1369Tyr
|
|
|
XM_011528652.2:c.3761T>A
|
XP_011526954.1:p.Phe1254Tyr
|
|
|
XM_017027704.1:c.3761T>A
|
XP_016883193.1:p.Phe1254Tyr
|
|
|
XM_017027705.1:c.3761T>A
|
XP_016883194.1:p.Phe1254Tyr
|
|
|
XM_017027706.1:c.3692T>A
|
XP_016883195.1:p.Phe1231Tyr
|
|
|
NM_015338.6:c.3845T>A
MANE Select
|
NP_056153.2:p.Phe1282Tyr
|
|
