ENST00000237596.7:c.1354A>T
MANE Select
|
ENSP00000237596.2:p.Ile452Phe
|
|
ENST00000237596.6:c.1354A>T
|
ENSP00000237596.2:p.Ile452Phe
|
|
ENST00000508588.5:c.-199+3219A>T
|
ENSP00000427131.1:n.-199+3219A>T
|
|
NM_000297.3:c.1354A>T
|
NP_000288.1:p.Ile452Phe
|
|
XM_011532028.1:c.1129A>T
|
XP_011530330.1:p.Ile377Phe
|
|
XM_011532029.1:c.634A>T
|
XP_011530331.1:p.Ile212Phe
|
|
XM_011532030.1:c.514A>T
|
XP_011530332.1:p.Ile172Phe
|
|
XR_244632.2:n.1449A>T
|
|
|
NR_156488.1:n.1441A>T
|
|
|
XM_011532028.2:c.1129A>T
|
XP_011530330.1:p.Ile377Phe
|
|
XM_011532030.2:c.514A>T
|
XP_011530332.1:p.Ile172Phe
|
|
NM_000297.4:c.1354A>T
MANE Select
|
NP_000288.1:p.Ile452Phe
|
|
NR_156488.2:n.1453A>T
|
|
|