ENST00000373631.8:c.3795G>T
MANE Select
|
ENSP00000362734.3:p.Val1265=
|
|
ENST00000373631.7:c.3795G>T
|
ENSP00000362734.3:p.Val1265=
|
|
ENST00000460253.1:c.2799G>T
|
ENSP00000435279.1:p.Val933=
|
|
NM_173689.6:c.3795G>T
|
NP_775960.4:p.Val1265=
|
|
NR_104603.1:n.2909G>T
|
|
|
XM_005251934.1:c.2799G>T
|
XP_005251991.1:p.Val933=
|
|
XM_011518556.1:c.3768G>T
|
XP_011516858.1:p.Val1256=
|
|
XM_011518557.1:c.3600G>T
|
XP_011516859.1:p.Val1200=
|
|
XM_011518558.1:c.3600G>T
|
XP_011516860.1:p.Val1200=
|
|
XM_005251934.3:c.2799G>T
|
XP_005251991.1:p.Val933=
|
|
XM_011518556.3:c.3768G>T
|
XP_011516858.1:p.Val1256=
|
|
XM_011518557.3:c.3600G>T
|
XP_011516859.1:p.Val1200=
|
|
XM_011518558.3:c.3600G>T
|
XP_011516860.1:p.Val1200=
|
|
NM_173689.7:c.3795G>T
MANE Select
|
NP_775960.4:p.Val1265=
|
|
NR_104603.2:n.2909G>T
|
|
|