ENST00000237596.7:c.1459T>C
MANE Select
|
ENSP00000237596.2:p.Tyr487His
|
|
ENST00000237596.6:c.1459T>C
|
ENSP00000237596.2:p.Tyr487His
|
|
ENST00000508588.5:c.-199+3324T>C
|
ENSP00000427131.1:n.-199+3324T>C
|
|
NM_000297.3:c.1459T>C
|
NP_000288.1:p.Tyr487His
|
|
XM_011532028.1:c.1234T>C
|
XP_011530330.1:p.Tyr412His
|
|
XM_011532029.1:c.739T>C
|
XP_011530331.1:p.Tyr247His
|
|
XM_011532030.1:c.619T>C
|
XP_011530332.1:p.Tyr207His
|
|
XR_244632.2:n.1554T>C
|
|
|
NR_156488.1:n.1546T>C
|
|
|
XM_011532028.2:c.1234T>C
|
XP_011530330.1:p.Tyr412His
|
|
XM_011532030.2:c.619T>C
|
XP_011530332.1:p.Tyr207His
|
|
NM_000297.4:c.1459T>C
MANE Select
|
NP_000288.1:p.Tyr487His
|
|
NR_156488.2:n.1558T>C
|
|
|