ENST00000382103.7:c.971T>G
MANE Select
|
ENSP00000371535.2:p.Ile324Ser
|
|
ENST00000680581.1:c.971T>G
|
ENSP00000506483.1:p.Ile324Ser
|
|
ENST00000680824.1:n.2187T>G
|
|
|
ENST00000681071.1:n.1263T>G
|
|
|
ENST00000681341.1:n.2112T>G
|
|
|
ENST00000681948.1:c.1226T>G
|
ENSP00000505991.1:p.Ile409Ser
|
|
ENST00000358971.7:c.*769T>G
|
ENSP00000351857.3:n.*769T>G
|
|
ENST00000382103.6:c.971T>G
|
ENSP00000371535.2:p.Ile324Ser
|
|
ENST00000503150.1:c.253T>G
|
|
|
ENST00000505513.1:n.271T>G
|
|
|
ENST00000514585.5:c.*672T>G
|
ENSP00000421880.1:n.*672T>G
|
|
NM_016955.3:c.971T>G
|
NP_058651.3:p.Ile324Ser
|
|
XM_005248168.2:c.734T>G
|
XP_005248225.1:p.Ile245Ser
|
|
XM_006713965.2:c.791T>G
|
XP_006714028.1:p.Ile264Ser
|
|
XM_011513846.1:c.968T>G
|
XP_011512148.1:p.Ile323Ser
|
|
XM_011513847.1:c.938T>G
|
XP_011512149.1:p.Ile313Ser
|
|
XM_011513848.1:c.791T>G
|
XP_011512150.1:p.Ile264Ser
|
|
XM_011513846.2:c.968T>G
|
XP_011512148.1:p.Ile323Ser
|
|
XM_011513847.2:c.938T>G
|
XP_011512149.1:p.Ile313Ser
|
|
XM_017008277.1:c.1226T>G
|
XP_016863766.1:p.Ile409Ser
|
|
XM_017008278.1:c.548T>G
|
XP_016863767.1:p.Ile183Ser
|
|
NM_016955.4:c.971T>G
MANE Select
|
NP_058651.3:p.Ile324Ser
|
|