ENST00000261819.8:c.1702T>C
MANE Select
|
ENSP00000261819.3:p.Leu568=
|
|
ENST00000261819.7:c.1702T>C
|
ENSP00000261819.3:p.Leu568=
|
|
ENST00000366333.3:n.914T>C
|
|
|
ENST00000441917.6:c.1366T>C
|
ENSP00000415061.2:p.Leu456=
|
|
ENST00000534976.5:n.2358T>C
|
|
|
ENST00000535482.1:c.700T>C
|
ENSP00000438754.1:p.Leu234=
|
|
ENST00000535641.5:n.1913T>C
|
|
|
ENST00000539079.5:c.1046T>C
|
|
|
ENST00000541887.5:c.1663T>C
|
ENSP00000439875.1:p.Leu555=
|
|
ENST00000544314.5:n.820T>C
|
|
|
ENST00000545218.5:n.945T>C
|
|
|
NM_001137559.1:c.1366T>C
|
NP_001131031.1:p.Leu456=
|
|
NM_016237.4:c.1702T>C
|
NP_057321.2:p.Leu568=
|
|
XM_005253900.2:c.1663T>C
|
XP_005253957.1:p.Leu555=
|
|
XM_006719449.1:c.508T>C
|
XP_006719512.1:p.Leu170=
|
|
NM_001330489.1:c.1663T>C
|
NP_001317418.1:p.Leu555=
|
|
XM_017019423.2:c.508T>C
|
XP_016874912.1:p.Leu170=
|
|
XM_017019424.2:c.508T>C
|
XP_016874913.1:p.Leu170=
|
|
NM_016237.5:c.1702T>C
MANE Select
|
NP_057321.2:p.Leu568=
|
|
NM_001330489.2:c.1663T>C
|
NP_001317418.1:p.Leu555=
|
|