ENST00000393655.4:c.542C>G
MANE Select
|
ENSP00000377265.2:p.Ser181Ter
|
|
ENST00000344788.7:c.536C>G
|
ENSP00000342252.3:p.Ser179Ter
|
|
ENST00000393655.3:c.542C>G
|
ENSP00000377265.2:p.Ser181Ter
|
|
NM_003221.3:c.542C>G
|
NP_003212.2:p.Ser181Ter
|
|
XM_006715176.2:c.542C>G
|
XP_006715239.1:p.Ser181Ter
|
|
XM_006715177.2:c.488C>G
|
XP_006715240.1:p.Ser163Ter
|
|
XM_011514834.1:c.569C>G
|
XP_011513136.1:p.Ser190Ter
|
|
XM_011514835.1:c.569C>G
|
XP_011513137.1:p.Ser190Ter
|
|
XM_011514836.1:c.569C>G
|
XP_011513138.1:p.Ser190Ter
|
|
XM_011514837.1:c.569C>G
|
XP_011513139.1:p.Ser190Ter
|
|
XM_011514837.2:c.569C>G
|
XP_011513139.1:p.Ser190Ter
|
|
XM_017011233.1:c.707C>G
|
XP_016866722.1:p.Ser236Ter
|
|
XM_017011234.1:c.671C>G
|
XP_016866723.1:p.Ser224Ter
|
|
XM_017011235.2:c.83C>G
|
XP_016866724.1:p.Ser28Ter
|
|
NM_003221.4:c.542C>G
MANE Select
|
NP_003212.2:p.Ser181Ter
|
|