ENST00000547103.7:c.6246T>C
MANE Select
|
ENSP00000447211.2:p.Leu2082=
|
|
ENST00000642294.1:c.186T>C
|
ENSP00000493572.1:p.Leu62=
|
|
ENST00000646859.1:c.6111T>C
|
ENSP00000496036.1:p.Leu2037=
|
|
ENST00000298820.7:c.1527+104T>C
|
|
|
ENST00000458043.6:c.6219T>C
|
ENSP00000400895.2:p.Leu2073=
|
|
ENST00000546620.5:n.502T>C
|
|
|
ENST00000547103.5:c.6183T>C
|
ENSP00000447211.1:p.Leu2061=
|
|
ENST00000550182.2:c.270T>C
|
ENSP00000449641.1:p.Leu90=
|
|
ENST00000551340.5:c.374T>C
|
|
|
NM_173591.3:c.6219T>C
|
NP_775862.3:p.Leu2073=
|
|
XM_005268802.2:c.6270T>C
|
XP_005268859.1:p.Leu2090=
|
|
XM_011538191.1:c.6270T>C
|
XP_011536493.1:p.Leu2090=
|
|
XM_011538192.1:c.6117T>C
|
XP_011536494.1:p.Leu2039=
|
|
XM_011538193.1:c.5904T>C
|
XP_011536495.1:p.Leu1968=
|
|
XM_005268802.3:c.6270T>C
|
XP_005268859.1:p.Leu2090=
|
|
XM_011538192.2:c.6117T>C
|
XP_011536494.1:p.Leu2039=
|
|
NM_001368062.1:c.6084T>C
|
NP_001354991.1:p.Leu2028=
|
|
NM_001368062.3:c.6111T>C
|
NP_001354991.2:p.Leu2037=
|
|
NM_001378609.3:c.6246T>C
MANE Select
|
NP_001365538.2:p.Leu2082=
|
|
NM_001378610.3:c.6246T>C
|
NP_001365539.2:p.Leu2082=
|
|
NM_173591.7:c.6246T>C
|
NP_775862.4:p.Leu2082=
|
|