ENST00000675785.2:c.997C>T
|
ENSP00000502019.1:p.Pro333Ser
|
|
ENST00000373477.9:c.1144C>T
MANE Select
|
ENSP00000362576.4:p.Pro382Ser
|
|
ENST00000674629.1:c.*692C>T
|
ENSP00000502470.1:n.*692C>T
|
|
ENST00000674654.1:c.*1104C>T
|
ENSP00000501729.1:n.*1104C>T
|
|
ENST00000675785.1:c.997C>T
|
ENSP00000502019.1:p.Pro333Ser
|
|
ENST00000676297.1:c.*1318C>T
|
ENSP00000501596.1:n.*1318C>T
|
|
ENST00000373477.8:c.1144C>T
|
ENSP00000362576.4:p.Pro382Ser
|
|
ENST00000469100.5:n.1060C>T
|
|
|
ENST00000478828.1:n.611C>T
|
|
|
ENST00000487404.5:n.1454C>T
|
|
|
ENST00000490826.1:n.437C>T
|
|
|
ENST00000616261.1:c.1143C>T
|
ENSP00000484192.1:p.Thr381=
|
|
NM_003680.3:c.1144C>T , LRG_273t1:c.1144C>T
|
NP_003671.1:p.Pro382Ser
|
|
XM_011542347.1:c.514C>T
|
XP_011540649.1:p.Pro172Ser
|
|
XM_011542348.1:c.514C>T
|
XP_011540650.1:p.Pro172Ser
|
|
XM_011542347.2:c.514C>T
|
XP_011540649.1:p.Pro172Ser
|
|
XM_017002651.2:c.514C>T
|
XP_016858140.1:p.Pro172Ser
|
|
NM_003680.4:c.1144C>T
MANE Select
|
NP_003671.1:p.Pro382Ser
|
|