ENST00000547103.7:c.6183G>C
MANE Select
|
ENSP00000447211.2:p.Val2061=
|
|
ENST00000642294.1:c.123G>C
|
ENSP00000493572.1:p.Val41=
|
|
ENST00000646859.1:c.6048G>C
|
ENSP00000496036.1:p.Val2016=
|
|
ENST00000298820.7:c.1484G>C
|
|
|
ENST00000458043.6:c.6156G>C
|
ENSP00000400895.2:p.Val2052=
|
|
ENST00000546620.5:n.439G>C
|
|
|
ENST00000547103.5:c.6120G>C
|
ENSP00000447211.1:p.Val2040=
|
|
ENST00000550182.2:c.207G>C
|
ENSP00000449641.1:p.Val69=
|
|
ENST00000551340.5:c.311G>C
|
|
|
NM_173591.3:c.6156G>C
|
NP_775862.3:p.Val2052=
|
|
XM_005268802.2:c.6207G>C
|
XP_005268859.1:p.Val2069=
|
|
XM_011538191.1:c.6207G>C
|
XP_011536493.1:p.Val2069=
|
|
XM_011538192.1:c.6054G>C
|
XP_011536494.1:p.Val2018=
|
|
XM_011538193.1:c.5841G>C
|
XP_011536495.1:p.Val1947=
|
|
XM_005268802.3:c.6207G>C
|
XP_005268859.1:p.Val2069=
|
|
XM_011538192.2:c.6054G>C
|
XP_011536494.1:p.Val2018=
|
|
NM_001368062.1:c.6021G>C
|
NP_001354991.1:p.Val2007=
|
|
NM_001368062.3:c.6048G>C
|
NP_001354991.2:p.Val2016=
|
|
NM_001378609.3:c.6183G>C
MANE Select
|
NP_001365538.2:p.Val2061=
|
|
NM_001378610.3:c.6183G>C
|
NP_001365539.2:p.Val2061=
|
|
NM_173591.7:c.6183G>C
|
NP_775862.4:p.Val2061=
|
|