ENST00000373631.8:c.3274G=
MANE Select
|
ENSP00000362734.3:p.Glu1092=
|
|
ENST00000359999.7:c.3274G=
|
ENSP00000353092.3:p.Glu1092=
|
|
ENST00000373631.7:c.3274G=
|
ENSP00000362734.3:p.Glu1092=
|
|
ENST00000460253.1:c.2278G=
|
ENSP00000435279.1:p.Glu760=
|
|
NM_173689.6:c.3274G=
|
NP_775960.4:p.Glu1092=
|
|
NR_104603.1:n.2388G=
|
|
|
XM_005251934.1:c.2278G=
|
XP_005251991.1:p.Glu760=
|
|
XM_011518556.1:c.3247G=
|
XP_011516858.1:p.Glu1083=
|
|
XM_011518557.1:c.3079G=
|
XP_011516859.1:p.Glu1027=
|
|
XM_011518558.1:c.3079G=
|
XP_011516860.1:p.Glu1027=
|
|
XM_005251934.3:c.2278G=
|
XP_005251991.1:p.Glu760=
|
|
XM_011518556.3:c.3247G=
|
XP_011516858.1:p.Glu1083=
|
|
XM_011518557.3:c.3079G=
|
XP_011516859.1:p.Glu1027=
|
|
XM_011518558.3:c.3079G=
|
XP_011516860.1:p.Glu1027=
|
|
NM_173689.7:c.3274G=
MANE Select
|
NP_775960.4:p.Glu1092=
|
|
NR_104603.2:n.2388G=
|
|
|