ENST00000675785.2:c.1100A=
|
ENSP00000502019.1:p.Gln367=
|
|
ENST00000373477.9:c.1247A=
MANE Select
|
ENSP00000362576.4:p.Gln416=
|
|
ENST00000674629.1:c.*795A=
|
ENSP00000502470.1:n.*795A=
|
|
ENST00000674654.1:c.*1207A=
|
ENSP00000501729.1:n.*1207A=
|
|
ENST00000675785.1:c.1100A=
|
ENSP00000502019.1:p.Gln367=
|
|
ENST00000676297.1:c.*1421A=
|
ENSP00000501596.1:n.*1421A=
|
|
ENST00000373477.8:c.1247A=
|
ENSP00000362576.4:p.Gln416=
|
|
ENST00000469100.5:n.1163A=
|
|
|
ENST00000478828.1:n.714A=
|
|
|
ENST00000487404.5:n.1557A=
|
|
|
ENST00000490826.1:n.540A=
|
|
|
NM_003680.3:c.1247A= , LRG_273t1:c.1247A=
|
NP_003671.1:p.Gln416=
|
|
XM_011542347.1:c.617A=
|
XP_011540649.1:p.Gln206=
|
|
XM_011542348.1:c.617A=
|
XP_011540650.1:p.Gln206=
|
|
XM_011542347.2:c.617A=
|
XP_011540649.1:p.Gln206=
|
|
XM_017002651.2:c.617A=
|
XP_016858140.1:p.Gln206=
|
|
NM_003680.4:c.1247A=
MANE Select
|
NP_003671.1:p.Gln416=
|
|