ENST00000237596.7:c.1457A>T
MANE Select
|
ENSP00000237596.2:p.Tyr486Phe
|
|
ENST00000237596.6:c.1457A>T
|
ENSP00000237596.2:p.Tyr486Phe
|
|
ENST00000508588.5:c.-199+3322A>T
|
ENSP00000427131.1:n.-199+3322A>T
|
|
NM_000297.3:c.1457A>T
|
NP_000288.1:p.Tyr486Phe
|
|
XM_011532028.1:c.1232A>T
|
XP_011530330.1:p.Tyr411Phe
|
|
XM_011532029.1:c.737A>T
|
XP_011530331.1:p.Tyr246Phe
|
|
XM_011532030.1:c.617A>T
|
XP_011530332.1:p.Tyr206Phe
|
|
XR_244632.2:n.1552A>T
|
|
|
NR_156488.1:n.1544A>T
|
|
|
XM_011532028.2:c.1232A>T
|
XP_011530330.1:p.Tyr411Phe
|
|
XM_011532030.2:c.617A>T
|
XP_011530332.1:p.Tyr206Phe
|
|
NM_000297.4:c.1457A>T
MANE Select
|
NP_000288.1:p.Tyr486Phe
|
|
NR_156488.2:n.1556A>T
|
|
|