ENST00000261819.8:c.1731A>T
MANE Select
|
ENSP00000261819.3:p.Thr577=
|
|
ENST00000261819.7:c.1731A>T
|
ENSP00000261819.3:p.Thr577=
|
|
ENST00000441917.6:c.1395A>T
|
ENSP00000415061.2:p.Thr465=
|
|
ENST00000534976.5:n.2387A>T
|
|
|
ENST00000535482.1:c.729A>T
|
ENSP00000438754.1:p.Thr243=
|
|
ENST00000535641.5:n.1942A>T
|
|
|
ENST00000539079.5:c.1075A>T
|
|
|
ENST00000541887.5:c.1692A>T
|
ENSP00000439875.1:p.Thr564=
|
|
ENST00000544314.5:n.849A>T
|
|
|
ENST00000545218.5:n.974A>T
|
|
|
NM_001137559.1:c.1395A>T
|
NP_001131031.1:p.Thr465=
|
|
NM_016237.4:c.1731A>T
|
NP_057321.2:p.Thr577=
|
|
XM_005253900.2:c.1692A>T
|
XP_005253957.1:p.Thr564=
|
|
XM_006719449.1:c.537A>T
|
XP_006719512.1:p.Thr179=
|
|
NM_001330489.1:c.1692A>T
|
NP_001317418.1:p.Thr564=
|
|
XM_017019423.2:c.537A>T
|
XP_016874912.1:p.Thr179=
|
|
XM_017019424.2:c.537A>T
|
XP_016874913.1:p.Thr179=
|
|
NM_016237.5:c.1731A>T
MANE Select
|
NP_057321.2:p.Thr577=
|
|
NM_001330489.2:c.1692A>T
|
NP_001317418.1:p.Thr564=
|
|