ENST00000350026.11:c.3445T>C
|
ENSP00000055163.8:p.Phe1149Leu
|
|
ENST00000414678.8:c.3514T>C
|
ENSP00000412835.3:p.Phe1172Leu
|
|
ENST00000637015.2:c.3733T>C
|
ENSP00000489729.2:p.Phe1245Leu
|
|
ENST00000319584.11:c.1618T>C
|
ENSP00000313006.7:p.Phe540Leu
|
|
ENST00000346085.10:c.3484T>C
|
ENSP00000344546.5:p.Phe1162Leu
|
|
ENST00000350026.10:c.3196T>C
|
ENSP00000055163.7:p.Phe1066Leu
|
|
ENST00000414678.7:c.1762T>C
|
ENSP00000412835.2:p.Phe588Leu
|
|
ENST00000635849.1:c.925T>C
|
ENSP00000490948.1:p.Phe309Leu
|
|
ENST00000635957.1:c.559T>C
|
ENSP00000490385.1:p.Phe187Leu
|
|
ENST00000636930.2:c.3604T>C
MANE Select
|
ENSP00000490491.2:p.Phe1202Leu
|
|
ENST00000636940.1:n.1601T>C
|
|
|
ENST00000637015.1:c.972T>C
|
|
|
ENST00000637568.1:c.886T>C
|
|
|
ENST00000637741.1:n.270T>C
|
|
|
ENST00000637810.1:c.946T>C
|
ENSP00000489636.1:p.Phe316Leu
|
|
ENST00000637904.1:c.1105T>C
|
ENSP00000490550.1:p.Phe369Leu
|
|
ENST00000647938.1:c.3235T>C
|
ENSP00000498155.1:p.Phe1079Leu
|
|
ENST00000319584.10:c.1621T>C
|
ENSP00000313006.6:p.Phe541Leu
|
|
ENST00000346085.9:c.3235T>C
|
ENSP00000344546.4:p.Phe1079Leu
|
|
ENST00000350026.9:c.3196T>C
|
ENSP00000055163.7:p.Phe1066Leu
|
|
ENST00000400790.3:c.397T>C
|
ENSP00000383596.3:p.Phe133Leu
|
|
ENST00000414678.6:c.1762T>C
|
ENSP00000412835.2:p.Phe588Leu
|
|
ENST00000478761.3:c.806T>C
|
|
|
NM_017519.2:c.3196T>C
|
NP_059989.2:p.Phe1066Leu
|
|
NM_020732.3:c.3235T>C
|
NP_065783.3:p.Phe1079Leu
|
|
XM_005267069.3:c.3355T>C
|
XP_005267126.2:p.Phe1119Leu
|
|
XM_011535984.1:c.2434T>C
|
XP_011534286.1:p.Phe812Leu
|
|
XM_011535985.1:c.2254T>C
|
XP_011534287.1:p.Phe752Leu
|
|
XM_011535986.1:c.2014T>C
|
XP_011534288.1:p.Phe672Leu
|
|
XM_011535987.1:c.1633T>C
|
XP_011534289.1:p.Phe545Leu
|
|
XM_011535988.1:c.496T>C
|
XP_011534290.1:p.Phe166Leu
|
|
NM_001346813.1:c.3355T>C
|
NP_001333742.1:p.Phe1119Leu
|
|
NM_001363725.1:c.1105T>C
|
NP_001350654.1:p.Phe369Leu
|
|
XM_011535984.2:c.3565T>C
|
XP_011534286.2:p.Phe1189Leu
|
|
XM_011535988.3:c.496T>C
|
XP_011534290.1:p.Phe166Leu
|
|
XM_017011103.2:c.3466T>C
|
XP_016866592.1:p.Phe1156Leu
|
|
XM_017011104.1:c.3436T>C
|
XP_016866593.1:p.Phe1146Leu
|
|
XM_017011105.2:c.3406T>C
|
XP_016866594.1:p.Phe1136Leu
|
|
XM_017011106.2:c.3277T>C
|
XP_016866595.1:p.Phe1093Leu
|
|
XM_017011107.2:c.3256T>C
|
XP_016866596.1:p.Phe1086Leu
|
|
XR_002956289.1:n.3648T>C
|
|
|
NM_001363725.2:c.1105T>C
|
NP_001350654.1:p.Phe369Leu
|
|
NM_001371656.1:c.3484T>C
|
NP_001358585.1:p.Phe1162Leu
|
|
NM_001374820.1:c.3484T>C
|
NP_001361749.1:p.Phe1162Leu
|
|
NM_001374828.1:c.3604T>C
MANE Select
|
NP_001361757.1:p.Phe1202Leu
|
|
NM_017519.3:c.3445T>C
|
NP_059989.3:p.Phe1149Leu
|
|