ENST00000337299.7:c.1324G>T
|
ENSP00000338213.6:p.Ala442Ser
|
|
ENST00000380518.8:c.1531G>T
MANE Select
|
ENSP00000369889.3:p.Ala511Ser
|
|
ENST00000337299.6:c.1324G>T
|
ENSP00000338213.6:p.Ala442Ser
|
|
ENST00000380518.7:c.1531G>T
|
ENSP00000369889.3:p.Ala511Ser
|
|
ENST00000493991.5:n.455G>T
|
|
|
NM_001844.4:c.1531G>T
|
NP_001835.3:p.Ala511Ser
|
|
NM_033150.2:c.1324G>T
|
NP_149162.2:p.Ala442Ser
|
|
XM_006719242.2:c.1675G>T
|
XP_006719305.2:p.Ala559Ser
|
|
XM_011537928.1:c.1675G>T
|
XP_011536230.1:p.Ala559Ser
|
|
XM_011537929.1:c.1675G>T
|
XP_011536231.1:p.Ala559Ser
|
|
XM_011537930.1:c.1675G>T
|
XP_011536232.1:p.Ala559Ser
|
|
XM_011537931.1:c.1675G>T
|
XP_011536233.1:p.Ala559Ser
|
|
XM_011537932.1:c.1675G>T
|
XP_011536234.1:p.Ala559Ser
|
|
XM_011537933.1:c.1675G>T
|
XP_011536235.1:p.Ala559Ser
|
|
XM_011537934.1:c.1672G>T
|
XP_011536236.1:p.Ala558Ser
|
|
XM_011537935.1:c.619G>T
|
XP_011536237.1:p.Ala207Ser
|
|
XM_017018828.1:c.1675G>T
|
XP_016874317.1:p.Ala559Ser
|
|
XM_017018829.1:c.1672G>T
|
XP_016874318.1:p.Ala558Ser
|
|
XM_017018830.1:c.1465G>T
|
XP_016874319.1:p.Ala489Ser
|
|
XM_017018831.2:c.985G>T
|
XP_016874320.1:p.Ala329Ser
|
|
NM_001844.5:c.1531G>T
MANE Select
|
NP_001835.3:p.Ala511Ser
|
|
NM_033150.3:c.1324G>T
|
NP_149162.2:p.Ala442Ser
|
|