ENST00000617695.5:c.7185T>C
|
ENSP00000481744.2:p.Asp2395=
|
|
ENST00000618192.5:c.7449T>C
|
ENSP00000480802.2:p.Asp2483=
|
|
ENST00000684985.1:n.816T>C
|
|
|
ENST00000688150.1:n.524T>C
|
|
|
ENST00000421865.3:c.7185T>C
MANE Select
|
ENSP00000400365.2:p.Asp2395=
|
|
ENST00000421865.2:c.7185T>C
|
ENSP00000400365.2:p.Asp2395=
|
|
ENST00000617695.4:c.7185T>C
|
ENSP00000481744.1:p.Asp2395=
|
|
ENST00000618192.4:c.7182T>C
|
ENSP00000480802.1:p.Asp2394=
|
|
NM_000426.3:c.7185T>C , LRG_409t1:c.7185T>C
|
NP_000417.2:p.Asp2395=
|
|
NM_001079823.1:c.7185T>C
|
NP_001073291.1:p.Asp2395=
|
|
XM_005266981.2:c.7449T>C
|
XP_005267038.1:p.Asp2483=
|
|
XM_005266982.2:c.7449T>C
|
XP_005267039.1:p.Asp2483=
|
|
XM_011535820.1:c.7443T>C
|
XP_011534122.1:p.Asp2481=
|
|
XM_005266981.3:c.7449T>C
|
XP_005267038.1:p.Asp2483=
|
|
XM_005266982.3:c.7449T>C
|
XP_005267039.1:p.Asp2483=
|
|
XM_011535820.2:c.7443T>C
|
XP_011534122.1:p.Asp2481=
|
|
XM_017010851.2:c.7455T>C
|
XP_016866340.1:p.Asp2485=
|
|
XM_017010852.1:c.5580T>C
|
XP_016866341.1:p.Asp1860=
|
|
NM_000426.4:c.7185T>C
MANE Select
|
NP_000417.3:p.Asp2395=
|
|
NM_001079823.2:c.7185T>C
|
NP_001073291.2:p.Asp2395=
|
|