ENST00000373631.8:c.3696C>G
MANE Select
|
ENSP00000362734.3:p.Ala1232=
|
|
ENST00000373631.7:c.3696C>G
|
ENSP00000362734.3:p.Ala1232=
|
|
ENST00000460253.1:c.2700C>G
|
ENSP00000435279.1:p.Ala900=
|
|
NM_173689.6:c.3696C>G
|
NP_775960.4:p.Ala1232=
|
|
NR_104603.1:n.2810C>G
|
|
|
XM_005251934.1:c.2700C>G
|
XP_005251991.1:p.Ala900=
|
|
XM_011518556.1:c.3669C>G
|
XP_011516858.1:p.Ala1223=
|
|
XM_011518557.1:c.3501C>G
|
XP_011516859.1:p.Ala1167=
|
|
XM_011518558.1:c.3501C>G
|
XP_011516860.1:p.Ala1167=
|
|
XM_005251934.3:c.2700C>G
|
XP_005251991.1:p.Ala900=
|
|
XM_011518556.3:c.3669C>G
|
XP_011516858.1:p.Ala1223=
|
|
XM_011518557.3:c.3501C>G
|
XP_011516859.1:p.Ala1167=
|
|
XM_011518558.3:c.3501C>G
|
XP_011516860.1:p.Ala1167=
|
|
NM_173689.7:c.3696C>G
MANE Select
|
NP_775960.4:p.Ala1232=
|
|
NR_104603.2:n.2810C>G
|
|
|