ENST00000675785.2:c.1013T>A
|
ENSP00000502019.1:p.Leu338Gln
|
|
ENST00000373477.9:c.1160T>A
MANE Select
|
ENSP00000362576.4:p.Leu387Gln
|
|
ENST00000674629.1:c.*708T>A
|
ENSP00000502470.1:n.*708T>A
|
|
ENST00000674654.1:c.*1120T>A
|
ENSP00000501729.1:n.*1120T>A
|
|
ENST00000675785.1:c.1013T>A
|
ENSP00000502019.1:p.Leu338Gln
|
|
ENST00000676297.1:c.*1334T>A
|
ENSP00000501596.1:n.*1334T>A
|
|
ENST00000373477.8:c.1160T>A
|
ENSP00000362576.4:p.Leu387Gln
|
|
ENST00000469100.5:n.1076T>A
|
|
|
ENST00000478828.1:n.627T>A
|
|
|
ENST00000487404.5:n.1470T>A
|
|
|
ENST00000490826.1:n.453T>A
|
|
|
ENST00000616261.1:c.1159T>A
|
ENSP00000484192.1:p.Cys387Ser
|
|
NM_003680.3:c.1160T>A , LRG_273t1:c.1160T>A
|
NP_003671.1:p.Leu387Gln
|
|
XM_011542347.1:c.530T>A
|
XP_011540649.1:p.Leu177Gln
|
|
XM_011542348.1:c.530T>A
|
XP_011540650.1:p.Leu177Gln
|
|
XM_011542347.2:c.530T>A
|
XP_011540649.1:p.Leu177Gln
|
|
XM_017002651.2:c.530T>A
|
XP_016858140.1:p.Leu177Gln
|
|
NM_003680.4:c.1160T>A
MANE Select
|
NP_003671.1:p.Leu387Gln
|
|