ENST00000237596.7:c.1421C>T
MANE Select
|
ENSP00000237596.2:p.Ala474Val
|
|
ENST00000237596.6:c.1421C>T
|
ENSP00000237596.2:p.Ala474Val
|
|
ENST00000508588.5:c.-199+3286C>T
|
ENSP00000427131.1:n.-199+3286C>T
|
|
NM_000297.3:c.1421C>T
|
NP_000288.1:p.Ala474Val
|
|
XM_011532028.1:c.1196C>T
|
XP_011530330.1:p.Ala399Val
|
|
XM_011532029.1:c.701C>T
|
XP_011530331.1:p.Ala234Val
|
|
XM_011532030.1:c.581C>T
|
XP_011530332.1:p.Ala194Val
|
|
XR_244632.2:n.1516C>T
|
|
|
NR_156488.1:n.1508C>T
|
|
|
XM_011532028.2:c.1196C>T
|
XP_011530330.1:p.Ala399Val
|
|
XM_011532030.2:c.581C>T
|
XP_011530332.1:p.Ala194Val
|
|
NM_000297.4:c.1421C>T
MANE Select
|
NP_000288.1:p.Ala474Val
|
|
NR_156488.2:n.1520C>T
|
|
|