ENST00000350026.11:c.4886T>A
|
ENSP00000055163.8:p.Phe1629Tyr
|
|
ENST00000414678.8:c.4955T>A
|
ENSP00000412835.3:p.Phe1652Tyr
|
|
ENST00000637015.2:c.5174T>A
|
ENSP00000489729.2:p.Phe1725Tyr
|
|
ENST00000346085.10:c.4925T>A
|
ENSP00000344546.5:p.Phe1642Tyr
|
|
ENST00000350026.10:c.4637T>A
|
ENSP00000055163.7:p.Phe1546Tyr
|
|
ENST00000414678.7:c.3203T>A
|
ENSP00000412835.2:p.Phe1068Tyr
|
|
ENST00000635849.1:c.2366T>A
|
ENSP00000490948.1:p.Phe789Tyr
|
|
ENST00000635957.1:c.1997T>A
|
ENSP00000490385.1:p.Phe666Tyr
|
|
ENST00000636227.1:n.3508T>A
|
|
|
ENST00000636254.1:n.965T>A
|
|
|
ENST00000636930.2:c.5045T>A
MANE Select
|
ENSP00000490491.2:p.Phe1682Tyr
|
|
ENST00000636940.1:n.3042T>A
|
|
|
ENST00000637015.1:c.2413T>A
|
|
|
ENST00000637568.1:c.2327T>A
|
|
|
ENST00000637741.1:n.1711T>A
|
|
|
ENST00000637810.1:c.2387T>A
|
ENSP00000489636.1:p.Phe796Tyr
|
|
ENST00000637904.1:c.2546T>A
|
ENSP00000490550.1:p.Phe849Tyr
|
|
ENST00000647938.1:c.4676T>A
|
ENSP00000498155.1:p.Phe1559Tyr
|
|
ENST00000346085.9:c.4676T>A
|
ENSP00000344546.4:p.Phe1559Tyr
|
|
ENST00000350026.9:c.4637T>A
|
ENSP00000055163.7:p.Phe1546Tyr
|
|
ENST00000414678.6:c.3203T>A
|
ENSP00000412835.2:p.Phe1068Tyr
|
|
NM_017519.2:c.4637T>A
|
NP_059989.2:p.Phe1546Tyr
|
|
NM_020732.3:c.4676T>A
|
NP_065783.3:p.Phe1559Tyr
|
|
XM_005267069.3:c.4796T>A
|
XP_005267126.2:p.Phe1599Tyr
|
|
XM_011535984.1:c.3875T>A
|
XP_011534286.1:p.Phe1292Tyr
|
|
XM_011535985.1:c.3695T>A
|
XP_011534287.1:p.Phe1232Tyr
|
|
XM_011535986.1:c.3455T>A
|
XP_011534288.1:p.Phe1152Tyr
|
|
XM_011535987.1:c.3074T>A
|
XP_011534289.1:p.Phe1025Tyr
|
|
XM_011535988.1:c.1937T>A
|
XP_011534290.1:p.Phe646Tyr
|
|
NM_001346813.1:c.4796T>A
|
NP_001333742.1:p.Phe1599Tyr
|
|
NM_001363725.1:c.2546T>A
|
NP_001350654.1:p.Phe849Tyr
|
|
XM_011535984.2:c.5006T>A
|
XP_011534286.2:p.Phe1669Tyr
|
|
XM_011535988.3:c.1937T>A
|
XP_011534290.1:p.Phe646Tyr
|
|
XM_017011103.2:c.4907T>A
|
XP_016866592.1:p.Phe1636Tyr
|
|
XM_017011104.1:c.4877T>A
|
XP_016866593.1:p.Phe1626Tyr
|
|
XM_017011105.2:c.4847T>A
|
XP_016866594.1:p.Phe1616Tyr
|
|
XM_017011106.2:c.4718T>A
|
XP_016866595.1:p.Phe1573Tyr
|
|
XM_017011107.2:c.4697T>A
|
XP_016866596.1:p.Phe1566Tyr
|
|
XR_002956289.1:n.4992T>A
|
|
|
NM_001363725.2:c.2546T>A
|
NP_001350654.1:p.Phe849Tyr
|
|
NM_001371656.1:c.4925T>A
|
NP_001358585.1:p.Phe1642Tyr
|
|
NM_001374820.1:c.4925T>A
|
NP_001361749.1:p.Phe1642Tyr
|
|
NM_001374828.1:c.5045T>A
MANE Select
|
NP_001361757.1:p.Phe1682Tyr
|
|
NM_017519.3:c.4886T>A
|
NP_059989.3:p.Phe1629Tyr
|
|