ENST00000478003.2:n.2056T>A
|
|
|
ENST00000682276.1:n.1673T>A
|
|
|
ENST00000682892.1:c.1775T>A
|
ENSP00000507214.1:p.Phe592Tyr
|
|
ENST00000682952.1:n.1867T>A
|
|
|
ENST00000684455.1:c.1441T>A
|
|
|
ENST00000684642.1:c.1625T>A
|
ENSP00000507355.1:p.Phe542Tyr
|
|
ENST00000684740.1:n.2406T>A
|
|
|
ENST00000303236.9:c.2228T>A
MANE Select
|
ENSP00000307235.3:p.Phe743Tyr
|
|
ENST00000652099.1:c.2422T>A
|
|
|
ENST00000652736.1:n.2104T>A
|
|
|
ENST00000303236.7:c.2228T>A
|
ENSP00000307235.3:p.Phe743Tyr
|
|
ENST00000415570.1:c.1865T>A
|
ENSP00000412076.1:p.Phe622Tyr
|
|
ENST00000419748.5:c.1775T>A
|
ENSP00000408325.1:p.Phe592Tyr
|
|
ENST00000470706.1:n.48+106T>A
|
|
|
NM_001313915.1:c.1775T>A
|
NP_001300844.1:p.Phe592Tyr
|
|
NM_004836.5:c.2228T>A
|
NP_004827.4:p.Phe743Tyr
|
|
NM_004836.6:c.2228T>A
|
NP_004827.4:p.Phe743Tyr
|
|
NR_110236.1:n.1392A>T
|
|
|
XM_005264649.3:c.1544T>A
|
XP_005264706.1:p.Phe515Tyr
|
|
XM_017005376.2:c.1544T>A
|
XP_016860865.1:p.Phe515Tyr
|
|
NM_004836.7:c.2228T>A
MANE Select
|
NP_004827.4:p.Phe743Tyr
|
|
NM_001313915.2:c.1775T>A
|
NP_001300844.1:p.Phe592Tyr
|
|