ENST00000261819.8:c.1700T>A
MANE Select
|
ENSP00000261819.3:p.Leu567Ter
|
|
ENST00000261819.7:c.1700T>A
|
ENSP00000261819.3:p.Leu567Ter
|
|
ENST00000366333.3:n.912T>A
|
|
|
ENST00000441917.6:c.1364T>A
|
ENSP00000415061.2:p.Leu455Ter
|
|
ENST00000534976.5:n.2356T>A
|
|
|
ENST00000535482.1:c.698T>A
|
ENSP00000438754.1:p.Leu233Ter
|
|
ENST00000535641.5:n.1911T>A
|
|
|
ENST00000539079.5:c.1044T>A
|
|
|
ENST00000541887.5:c.1661T>A
|
ENSP00000439875.1:p.Leu554Ter
|
|
ENST00000544314.5:n.818T>A
|
|
|
ENST00000545218.5:n.943T>A
|
|
|
NM_001137559.1:c.1364T>A
|
NP_001131031.1:p.Leu455Ter
|
|
NM_016237.4:c.1700T>A
|
NP_057321.2:p.Leu567Ter
|
|
XM_005253900.2:c.1661T>A
|
XP_005253957.1:p.Leu554Ter
|
|
XM_006719449.1:c.506T>A
|
XP_006719512.1:p.Leu169Ter
|
|
NM_001330489.1:c.1661T>A
|
NP_001317418.1:p.Leu554Ter
|
|
XM_017019423.2:c.506T>A
|
XP_016874912.1:p.Leu169Ter
|
|
XM_017019424.2:c.506T>A
|
XP_016874913.1:p.Leu169Ter
|
|
NM_016237.5:c.1700T>A
MANE Select
|
NP_057321.2:p.Leu567Ter
|
|
NM_001330489.2:c.1661T>A
|
NP_001317418.1:p.Leu554Ter
|
|