ENST00000237596.7:c.1172A>T
MANE Select
|
ENSP00000237596.2:p.Tyr391Phe
|
|
ENST00000237596.6:c.1172A>T
|
ENSP00000237596.2:p.Tyr391Phe
|
|
ENST00000506367.1:n.619A>T
|
|
|
ENST00000508588.5:c.-346A>T
|
ENSP00000427131.1:n.-346A>T
|
|
NM_000297.3:c.1172A>T
|
NP_000288.1:p.Tyr391Phe
|
|
XM_011532028.1:c.1095-3332A>T
|
XP_011530330.1:n.1095-3332A>T
|
|
XM_011532029.1:c.452A>T
|
XP_011530331.1:p.Tyr151Phe
|
|
XM_011532030.1:c.332A>T
|
XP_011530332.1:p.Tyr111Phe
|
|
XR_244632.2:n.1267A>T
|
|
|
NR_156488.1:n.1259A>T
|
|
|
XM_011532028.2:c.1095-3332A>T
|
XP_011530330.1:n.1095-3332A>T
|
|
XM_011532030.2:c.332A>T
|
XP_011530332.1:p.Tyr111Phe
|
|
NM_000297.4:c.1172A>T
MANE Select
|
NP_000288.1:p.Tyr391Phe
|
|
NR_156488.2:n.1271A>T
|
|
|