ENST00000237596.7:c.1458C>T
MANE Select
|
ENSP00000237596.2:p.Tyr486=
|
|
ENST00000237596.6:c.1458C>T
|
ENSP00000237596.2:p.Tyr486=
|
|
ENST00000508588.5:c.-199+3323C>T
|
ENSP00000427131.1:n.-199+3323C>T
|
|
NM_000297.3:c.1458C>T
|
NP_000288.1:p.Tyr486=
|
|
XM_011532028.1:c.1233C>T
|
XP_011530330.1:p.Tyr411=
|
|
XM_011532029.1:c.738C>T
|
XP_011530331.1:p.Tyr246=
|
|
XM_011532030.1:c.618C>T
|
XP_011530332.1:p.Tyr206=
|
|
XR_244632.2:n.1553C>T
|
|
|
NR_156488.1:n.1545C>T
|
|
|
XM_011532028.2:c.1233C>T
|
XP_011530330.1:p.Tyr411=
|
|
XM_011532030.2:c.618C>T
|
XP_011530332.1:p.Tyr206=
|
|
NM_000297.4:c.1458C>T
MANE Select
|
NP_000288.1:p.Tyr486=
|
|
NR_156488.2:n.1557C>T
|
|
|