ENST00000374479.4:c.1043T>C
MANE Select
|
ENSP00000363603.3:p.Val348Ala
|
|
ENST00000374479.3:c.1043T>C
|
ENSP00000363603.3:p.Val348Ala
|
|
NM_000147.4:c.1043T>C
|
NP_000138.2:p.Val348Ala
|
|
XM_005245821.1:c.668T>C
|
XP_005245878.1:p.Val223Ala
|
|
XM_011541167.1:c.410T>C
|
XP_011539469.1:p.Val137Ala
|
|
XM_005245821.3:c.668T>C
|
XP_005245878.1:p.Val223Ala
|
|
XM_011541167.3:c.410T>C
|
XP_011539469.1:p.Val137Ala
|
|
XM_017000905.2:c.740T>C
|
XP_016856394.1:p.Val247Ala
|
|
NM_000147.5:c.1043T>C
MANE Select
|
NP_000138.2:p.Val348Ala
|
|
NR_174379.1:n.1221T>C
|
|
|
NR_174380.1:n.1270T>C
|
|
|
NR_174381.1:n.1109T>C
|
|
|
NR_174382.1:n.1506T>C
|
|
|