ENST00000237596.7:c.1154C>T
MANE Select
|
ENSP00000237596.2:p.Thr385Ile
|
|
ENST00000237596.6:c.1154C>T
|
ENSP00000237596.2:p.Thr385Ile
|
|
ENST00000506367.1:n.601C>T
|
|
|
ENST00000508588.5:c.-364C>T
|
ENSP00000427131.1:n.-364C>T
|
|
NM_000297.3:c.1154C>T
|
NP_000288.1:p.Thr385Ile
|
|
XM_011532028.1:c.1095-3350C>T
|
XP_011530330.1:n.1095-3350C>T
|
|
XM_011532029.1:c.434C>T
|
XP_011530331.1:p.Thr145Ile
|
|
XM_011532030.1:c.314C>T
|
XP_011530332.1:p.Thr105Ile
|
|
XR_244632.2:n.1249C>T
|
|
|
NR_156488.1:n.1241C>T
|
|
|
XM_011532028.2:c.1095-3350C>T
|
XP_011530330.1:n.1095-3350C>T
|
|
XM_011532030.2:c.314C>T
|
XP_011530332.1:p.Thr105Ile
|
|
NM_000297.4:c.1154C>T
MANE Select
|
NP_000288.1:p.Thr385Ile
|
|
NR_156488.2:n.1253C>T
|
|
|