ENST00000237596.7:c.1472A>C
MANE Select
|
ENSP00000237596.2:p.Glu491Ala
|
|
ENST00000237596.6:c.1472A>C
|
ENSP00000237596.2:p.Glu491Ala
|
|
ENST00000508588.5:c.-199+3337A>C
|
ENSP00000427131.1:n.-199+3337A>C
|
|
NM_000297.3:c.1472A>C
|
NP_000288.1:p.Glu491Ala
|
|
XM_011532028.1:c.1247A>C
|
XP_011530330.1:p.Glu416Ala
|
|
XM_011532029.1:c.752A>C
|
XP_011530331.1:p.Glu251Ala
|
|
XM_011532030.1:c.632A>C
|
XP_011530332.1:p.Glu211Ala
|
|
XR_244632.2:n.1567A>C
|
|
|
NR_156488.1:n.1559A>C
|
|
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XM_011532028.2:c.1247A>C
|
XP_011530330.1:p.Glu416Ala
|
|
XM_011532030.2:c.632A>C
|
XP_011530332.1:p.Glu211Ala
|
|
NM_000297.4:c.1472A>C
MANE Select
|
NP_000288.1:p.Glu491Ala
|
|
NR_156488.2:n.1571A>C
|
|
|