ENST00000675785.2:c.1003G=
|
ENSP00000502019.1:p.Ala335=
|
|
ENST00000373477.9:c.1150G=
MANE Select
|
ENSP00000362576.4:p.Ala384=
|
|
ENST00000674629.1:c.*698G=
|
ENSP00000502470.1:n.*698G=
|
|
ENST00000674654.1:c.*1110G=
|
ENSP00000501729.1:n.*1110G=
|
|
ENST00000675785.1:c.1003G=
|
ENSP00000502019.1:p.Ala335=
|
|
ENST00000676297.1:c.*1324G=
|
ENSP00000501596.1:n.*1324G=
|
|
ENST00000373477.8:c.1150G=
|
ENSP00000362576.4:p.Ala384=
|
|
ENST00000469100.5:n.1066G=
|
|
|
ENST00000478828.1:n.617G=
|
|
|
ENST00000487404.5:n.1460G=
|
|
|
ENST00000490826.1:n.443G=
|
|
|
ENST00000616261.1:c.1149G=
|
ENSP00000484192.1:p.Met383=
|
|
NM_003680.3:c.1150G= , LRG_273t1:c.1150G=
|
NP_003671.1:p.Ala384=
|
|
XM_011542347.1:c.520G=
|
XP_011540649.1:p.Ala174=
|
|
XM_011542348.1:c.520G=
|
XP_011540650.1:p.Ala174=
|
|
XM_011542347.2:c.520G=
|
XP_011540649.1:p.Ala174=
|
|
XM_017002651.2:c.520G=
|
XP_016858140.1:p.Ala174=
|
|
NM_003680.4:c.1150G=
MANE Select
|
NP_003671.1:p.Ala384=
|
|