ENST00000382103.7:c.1013T>A
MANE Select
|
ENSP00000371535.2:p.Leu338Gln
|
|
ENST00000680581.1:c.1013T>A
|
ENSP00000506483.1:p.Leu338Gln
|
|
ENST00000680824.1:n.2229T>A
|
|
|
ENST00000681071.1:n.1305T>A
|
|
|
ENST00000681341.1:n.2154T>A
|
|
|
ENST00000681948.1:c.1268T>A
|
ENSP00000505991.1:p.Leu423Gln
|
|
ENST00000358971.7:c.*811T>A
|
ENSP00000351857.3:n.*811T>A
|
|
ENST00000382103.6:c.1013T>A
|
ENSP00000371535.2:p.Leu338Gln
|
|
ENST00000503150.1:c.295T>A
|
|
|
ENST00000505513.1:n.313T>A
|
|
|
ENST00000514585.5:c.*714T>A
|
ENSP00000421880.1:n.*714T>A
|
|
NM_016955.3:c.1013T>A
|
NP_058651.3:p.Leu338Gln
|
|
XM_005248168.2:c.776T>A
|
XP_005248225.1:p.Leu259Gln
|
|
XM_006713965.2:c.833T>A
|
XP_006714028.1:p.Leu278Gln
|
|
XM_011513846.1:c.1010T>A
|
XP_011512148.1:p.Leu337Gln
|
|
XM_011513847.1:c.980T>A
|
XP_011512149.1:p.Leu327Gln
|
|
XM_011513848.1:c.833T>A
|
XP_011512150.1:p.Leu278Gln
|
|
XM_011513846.2:c.1010T>A
|
XP_011512148.1:p.Leu337Gln
|
|
XM_011513847.2:c.980T>A
|
XP_011512149.1:p.Leu327Gln
|
|
XM_017008277.1:c.1268T>A
|
XP_016863766.1:p.Leu423Gln
|
|
XM_017008278.1:c.590T>A
|
XP_016863767.1:p.Leu197Gln
|
|
NM_016955.4:c.1013T>A
MANE Select
|
NP_058651.3:p.Leu338Gln
|
|