|
ENST00000706130.1:c.1205T>C
|
ENSP00000516215.1:p.Ile402Thr
|
|
|
ENST00000706151.1:c.413T>C
|
ENSP00000516234.1:p.Ile138Thr
|
|
|
ENST00000706153.1:n.1034T>C
|
|
|
|
ENST00000706154.1:n.672T>C
|
|
|
|
ENST00000706155.1:n.819T>C
|
|
|
|
ENST00000377770.8:c.1388T>C
MANE Select
|
ENSP00000367001.3:p.Ile463Thr
|
|
|
ENST00000332007.7:c.1202T>C
|
ENSP00000328226.3:p.Ile401Thr
|
|
|
ENST00000377770.7:c.1388T>C
|
ENSP00000367001.3:p.Ile463Thr
|
|
|
ENST00000404039.5:c.1196T>C
|
ENSP00000385578.1:p.Ile399Thr
|
|
|
ENST00000427557.1:c.1067T>C
|
ENSP00000397303.1:p.Ile356Thr
|
|
|
ENST00000471100.5:n.534T>C
|
|
|
|
NM_001039350.2:c.1196T>C
|
NP_001034439.1:p.Ile399Thr
|
|
|
NM_001290252.1:c.1067T>C
|
NP_001277181.1:p.Ile356Thr
|
|
|
NM_001936.4:c.1202T>C
|
NP_001927.3:p.Ile401Thr
|
|
|
NM_130797.3:c.1388T>C
|
NP_570629.2:p.Ile463Thr
|
|
|
XM_011515865.1:c.1196T>C
|
XP_011514167.1:p.Ile399Thr
|
|
|
XM_011515866.1:c.764T>C
|
XP_011514168.1:p.Ile255Thr
|
|
|
NM_001364497.1:c.1205T>C
|
NP_001351426.1:p.Ile402Thr
|
|
|
NM_001364498.1:c.1205T>C
|
NP_001351427.1:p.Ile402Thr
|
|
|
NM_001364499.1:c.1205T>C
|
NP_001351428.1:p.Ile402Thr
|
|
|
NM_001364500.1:c.1205T>C
|
NP_001351429.1:p.Ile402Thr
|
|
|
NR_157195.1:n.1838T>C
|
|
|
|
NR_157196.1:n.1538T>C
|
|
|
|
XM_017011812.2:c.764T>C
|
XP_016867301.1:p.Ile255Thr
|
|
|
NM_130797.4:c.1388T>C
MANE Select
|
NP_570629.2:p.Ile463Thr
|
|
|
NM_001039350.3:c.1196T>C
|
NP_001034439.1:p.Ile399Thr
|
|
|
NM_001290252.2:c.1067T>C
|
NP_001277181.1:p.Ile356Thr
|
|
|
NM_001364497.2:c.1205T>C
|
NP_001351426.1:p.Ile402Thr
|
|
|
NM_001364498.2:c.1205T>C
|
NP_001351427.1:p.Ile402Thr
|
|
|
NM_001364499.2:c.1205T>C
|
NP_001351428.1:p.Ile402Thr
|
|
|
NM_001364500.2:c.1205T>C
|
NP_001351429.1:p.Ile402Thr
|
|
|
NM_001936.5:c.1202T>C
|
NP_001927.3:p.Ile401Thr
|
|
|
NR_157196.2:n.1538T>C
|
|
|
|
NR_157195.2:n.1838T>C
|
|
|
