ENST00000237596.7:c.1484T>C
MANE Select
|
ENSP00000237596.2:p.Ile495Thr
|
|
ENST00000237596.6:c.1484T>C
|
ENSP00000237596.2:p.Ile495Thr
|
|
ENST00000508588.5:c.-199+3349T>C
|
ENSP00000427131.1:n.-199+3349T>C
|
|
NM_000297.3:c.1484T>C
|
NP_000288.1:p.Ile495Thr
|
|
XM_011532028.1:c.1259T>C
|
XP_011530330.1:p.Ile420Thr
|
|
XM_011532029.1:c.764T>C
|
XP_011530331.1:p.Ile255Thr
|
|
XM_011532030.1:c.644T>C
|
XP_011530332.1:p.Ile215Thr
|
|
XR_244632.2:n.1579T>C
|
|
|
NR_156488.1:n.1571T>C
|
|
|
XM_011532028.2:c.1259T>C
|
XP_011530330.1:p.Ile420Thr
|
|
XM_011532030.2:c.644T>C
|
XP_011530332.1:p.Ile215Thr
|
|
NM_000297.4:c.1484T>C
MANE Select
|
NP_000288.1:p.Ile495Thr
|
|
NR_156488.2:n.1583T>C
|
|
|