ENST00000675785.2:c.1031A>C
|
ENSP00000502019.1:p.Asp344Ala
|
|
ENST00000373477.9:c.1178A>C
MANE Select
|
ENSP00000362576.4:p.Asp393Ala
|
|
ENST00000674629.1:c.*726A>C
|
ENSP00000502470.1:n.*726A>C
|
|
ENST00000674654.1:c.*1138A>C
|
ENSP00000501729.1:n.*1138A>C
|
|
ENST00000675785.1:c.1031A>C
|
ENSP00000502019.1:p.Asp344Ala
|
|
ENST00000676297.1:c.*1352A>C
|
ENSP00000501596.1:n.*1352A>C
|
|
ENST00000373477.8:c.1178A>C
|
ENSP00000362576.4:p.Asp393Ala
|
|
ENST00000469100.5:n.1094A>C
|
|
|
ENST00000478828.1:n.645A>C
|
|
|
ENST00000487404.5:n.1488A>C
|
|
|
ENST00000490826.1:n.471A>C
|
|
|
NM_003680.3:c.1178A>C , LRG_273t1:c.1178A>C
|
NP_003671.1:p.Asp393Ala
|
|
XM_011542347.1:c.548A>C
|
XP_011540649.1:p.Asp183Ala
|
|
XM_011542348.1:c.548A>C
|
XP_011540650.1:p.Asp183Ala
|
|
XM_011542347.2:c.548A>C
|
XP_011540649.1:p.Asp183Ala
|
|
XM_017002651.2:c.548A>C
|
XP_016858140.1:p.Asp183Ala
|
|
NM_003680.4:c.1178A>C
MANE Select
|
NP_003671.1:p.Asp393Ala
|
|