|
ENST00000316673.9:c.420C>A
MANE Select
|
ENSP00000315180.4:p.Ser140=
|
|
|
ENST00000316099.10:c.486C>A
|
ENSP00000312987.3:p.Ser162=
|
|
|
ENST00000619550.5:c.460C>A
|
|
|
|
ENST00000683148.1:n.462C>A
|
|
|
|
ENST00000683657.1:n.1610C>A
|
|
|
|
ENST00000316099.9:c.486C>A
|
ENSP00000312987.3:p.Ser162=
|
|
|
ENST00000316099.8:c.486C>A
|
ENSP00000312987.3:p.Ser162=
|
|
|
ENST00000316673.8:c.420C>A
|
ENSP00000315180.4:p.Ser140=
|
|
|
ENST00000372920.1:c.*253C>A
|
ENSP00000362011.1:n.*253C>A
|
|
|
ENST00000415691.2:c.486C>A
|
ENSP00000412111.1:p.Ser162=
|
|
|
ENST00000443598.6:c.486C>A
|
ENSP00000410911.2:p.Ser162=
|
|
|
ENST00000457232.5:c.420C>A
|
ENSP00000396216.1:p.Ser140=
|
|
|
ENST00000609795.5:c.420C>A
|
ENSP00000476609.1:p.Ser140=
|
|
|
ENST00000619550.4:c.411C>A
|
ENSP00000481331.1:p.Ser137=
|
|
|
NM_000457.4:c.486C>A , LRG_483t2:c.486C>A
|
NP_000448.3:p.Ser162=
|
|
|
NM_001030003.2:c.420C>A
|
NP_001025174.1:p.Ser140=
|
|
|
NM_001030004.2:c.420C>A
|
NP_001025175.1:p.Ser140=
|
|
|
NM_001258355.1:c.465C>A
|
NP_001245284.1:p.Ser155=
|
|
|
NM_001287182.1:c.411C>A
|
NP_001274111.1:p.Ser137=
|
|
|
NM_001287183.1:c.411C>A , LRG_483t3:c.411C>A
|
NP_001274112.1:p.Ser137=
|
|
|
NM_001287184.1:c.411C>A
|
NP_001274113.1:p.Ser137=
|
|
|
NM_175914.4:c.420C>A , LRG_483t1:c.420C>A
|
NP_787110.2:p.Ser140=
|
|
|
NM_178849.2:c.486C>A
|
NP_849180.1:p.Ser162=
|
|
|
NM_178850.2:c.486C>A
|
NP_849181.1:p.Ser162=
|
|
|
XM_005260407.2:c.603C>A
|
XP_005260464.1:p.Ser201=
|
|
|
XM_011528797.1:c.534C>A
|
XP_011527099.1:p.Ser178=
|
|
|
XM_011528798.1:c.534C>A
|
XP_011527100.1:p.Ser178=
|
|
|
XM_005260407.4:c.603C>A
|
XP_005260464.1:p.Ser201=
|
|
|
NM_001030003.3:c.420C>A
|
NP_001025174.1:p.Ser140=
|
|
|
NM_001030004.3:c.420C>A
|
NP_001025175.1:p.Ser140=
|
|
|
NM_001258355.2:c.465C>A
|
NP_001245284.1:p.Ser155=
|
|
|
NM_001287182.2:c.411C>A
|
NP_001274111.1:p.Ser137=
|
|
|
NM_001287184.2:c.411C>A
|
NP_001274113.1:p.Ser137=
|
|
|
NM_178849.3:c.486C>A
|
NP_849180.1:p.Ser162=
|
|
|
NM_178850.3:c.486C>A
|
NP_849181.1:p.Ser162=
|
|
|
NM_000457.5:c.486C>A
|
NP_000448.3:p.Ser162=
|
|
|
NM_000457.6:c.486C>A
|
NP_000448.3:p.Ser162=
|
|
|
NM_001287183.2:c.411C>A
|
NP_001274112.1:p.Ser137=
|
|
|
NM_175914.5:c.420C>A
MANE Select
|
NP_787110.2:p.Ser140=
|
|
