ENST00000580876.6:c.156C>A
(CRHR1)
|
ENSP00000516345.1:p.Arg52=
|
|
ENST00000580955.6:n.896C>A
(CRHR1)
|
|
|
ENST00000705340.1:n.956C>A
(CRHR1)
|
|
|
ENST00000705341.1:c.*358C>A
(CRHR1)
|
ENSP00000516114.1:n.*358C>A
|
|
ENST00000705342.1:n.781C>A
(CRHR1)
|
|
|
ENST00000705343.1:n.921C>A
(CRHR1)
|
|
|
ENST00000705344.1:n.485C>A
(CRHR1)
|
|
|
ENST00000314537.10:c.681C>A
(CRHR1)
MANE Select
|
ENSP00000326060.6:p.Arg227=
|
|
ENST00000293493.11:c.768C>A
(CRHR1)
|
ENSP00000293493.8:p.Arg256=
|
|
ENST00000314537.9:c.681C>A
(CRHR1)
|
ENSP00000326060.5:p.Arg227=
|
|
ENST00000339069.9:c.378C>A
(CRHR1)
|
ENSP00000340522.6:p.Arg126=
|
|
ENST00000347197.9:c.*158C>A
(CRHR1)
|
ENSP00000239167.7:n.*158C>A
|
|
ENST00000352855.9:c.561C>A
(CRHR1)
|
ENSP00000344068.5:p.Arg187=
|
|
ENST00000398285.7:c.768C>A
(CRHR1)
|
ENSP00000381333.3:p.Arg256=
|
|
ENST00000577353.5:c.681C>A
(CRHR1)
|
ENSP00000462016.1:p.Arg227=
|
|
ENST00000581479.1:n.143C>A
(CRHR1)
|
|
|
ENST00000582766.5:n.739C>A
(CRHR1)
|
|
|
ENST00000583888.1:c.339+328C>A
(CRHR1)
|
ENSP00000462553.1:n.339+328C>A
|
|
ENST00000619154.4:c.*10C>A
(CRHR1)
|
ENSP00000484545.1:n.*10C>A
|
|
ENST00000634540.1:c.156C>A
(LINC02210-CRHR1)
|
ENSP00000488912.1:p.Arg52=
|
|
NM_001145146.1:c.768C>A
(CRHR1)
|
NP_001138618.1:p.Arg256=
|
|
NM_001145147.1:c.561C>A
(CRHR1)
|
NP_001138619.1:p.Arg187=
|
|
NM_001145148.1:c.681C>A
(CRHR1)
|
NP_001138620.1:p.Arg227=
|
|
NM_001256299.2:c.156C>A
(LINC02210-CRHR1)
|
NP_001243228.1:p.Arg52=
|
|
NM_001303016.1:c.378C>A
(LINC02210-CRHR1)
|
NP_001289945.1:p.Arg126=
|
|
NM_001303018.1:c.156C>A
(CRHR1)
|
NP_001289947.1:p.Arg52=
|
|
NM_001303020.1:c.378C>A
(CRHR1)
|
NP_001289949.1:p.Arg126=
|
|
NM_004382.4:c.681C>A
(CRHR1)
|
NP_004373.2:p.Arg227=
|
|
NM_001145146.2:c.768C>A
(CRHR1)
|
NP_001138618.1:p.Arg256=
|
|
NM_001145147.2:c.561C>A
(CRHR1)
|
NP_001138619.1:p.Arg187=
|
|
NM_001145148.2:c.681C>A
(CRHR1)
|
NP_001138620.1:p.Arg227=
|
|
NM_001256299.3:c.156C>A
(LINC02210-CRHR1)
|
NP_001243228.1:p.Arg52=
|
|
NM_001303018.2:c.156C>A
(CRHR1)
|
NP_001289947.1:p.Arg52=
|
|
NM_004382.5:c.681C>A
(CRHR1)
MANE Select
|
NP_004373.2:p.Arg227=
|
|
NM_001303020.2:c.378C>A
(CRHR1)
|
NP_001289949.1:p.Arg126=
|
|