ENST00000580876.6:c.153G>A
(CRHR1)
|
ENSP00000516345.1:p.Leu51=
|
|
ENST00000580955.6:n.893G>A
(CRHR1)
|
|
|
ENST00000705340.1:n.953G>A
(CRHR1)
|
|
|
ENST00000705341.1:c.*355G>A
(CRHR1)
|
ENSP00000516114.1:n.*355G>A
|
|
ENST00000705342.1:n.778G>A
(CRHR1)
|
|
|
ENST00000705343.1:n.918G>A
(CRHR1)
|
|
|
ENST00000705344.1:n.482G>A
(CRHR1)
|
|
|
ENST00000314537.10:c.678G>A
(CRHR1)
MANE Select
|
ENSP00000326060.6:p.Leu226=
|
|
ENST00000293493.11:c.765G>A
(CRHR1)
|
ENSP00000293493.8:p.Leu255=
|
|
ENST00000314537.9:c.678G>A
(CRHR1)
|
ENSP00000326060.5:p.Leu226=
|
|
ENST00000339069.9:c.375G>A
(CRHR1)
|
ENSP00000340522.6:p.Leu125=
|
|
ENST00000347197.9:c.*155G>A
(CRHR1)
|
ENSP00000239167.7:n.*155G>A
|
|
ENST00000352855.9:c.558G>A
(CRHR1)
|
ENSP00000344068.5:p.Leu186=
|
|
ENST00000398285.7:c.765G>A
(CRHR1)
|
ENSP00000381333.3:p.Leu255=
|
|
ENST00000577353.5:c.678G>A
(CRHR1)
|
ENSP00000462016.1:p.Leu226=
|
|
ENST00000581479.1:n.140G>A
(CRHR1)
|
|
|
ENST00000582766.5:n.736G>A
(CRHR1)
|
|
|
ENST00000583888.1:c.339+325G>A
(CRHR1)
|
ENSP00000462553.1:n.339+325G>A
|
|
ENST00000619154.4:c.*7G>A
(CRHR1)
|
ENSP00000484545.1:n.*7G>A
|
|
ENST00000634540.1:c.153G>A
(LINC02210-CRHR1)
|
ENSP00000488912.1:p.Leu51=
|
|
NM_001145146.1:c.765G>A
(CRHR1)
|
NP_001138618.1:p.Leu255=
|
|
NM_001145147.1:c.558G>A
(CRHR1)
|
NP_001138619.1:p.Leu186=
|
|
NM_001145148.1:c.678G>A
(CRHR1)
|
NP_001138620.1:p.Leu226=
|
|
NM_001256299.2:c.153G>A
(LINC02210-CRHR1)
|
NP_001243228.1:p.Leu51=
|
|
NM_001303016.1:c.375G>A
(LINC02210-CRHR1)
|
NP_001289945.1:p.Leu125=
|
|
NM_001303018.1:c.153G>A
(CRHR1)
|
NP_001289947.1:p.Leu51=
|
|
NM_001303020.1:c.375G>A
(CRHR1)
|
NP_001289949.1:p.Leu125=
|
|
NM_004382.4:c.678G>A
(CRHR1)
|
NP_004373.2:p.Leu226=
|
|
NM_001145146.2:c.765G>A
(CRHR1)
|
NP_001138618.1:p.Leu255=
|
|
NM_001145147.2:c.558G>A
(CRHR1)
|
NP_001138619.1:p.Leu186=
|
|
NM_001145148.2:c.678G>A
(CRHR1)
|
NP_001138620.1:p.Leu226=
|
|
NM_001256299.3:c.153G>A
(LINC02210-CRHR1)
|
NP_001243228.1:p.Leu51=
|
|
NM_001303018.2:c.153G>A
(CRHR1)
|
NP_001289947.1:p.Leu51=
|
|
NM_004382.5:c.678G>A
(CRHR1)
MANE Select
|
NP_004373.2:p.Leu226=
|
|
NM_001303020.2:c.375G>A
(CRHR1)
|
NP_001289949.1:p.Leu125=
|
|