ENST00000397195.10:c.995T>C
MANE Select
|
ENSP00000380378.4:p.Met332Thr
|
|
ENST00000571495.2:n.2080T>C
|
|
|
ENST00000674608.1:c.1049T>C
|
ENSP00000501976.1:p.Met350Thr
|
|
ENST00000674717.1:c.800T>C
|
ENSP00000501931.1:p.Met267Thr
|
|
ENST00000675084.1:n.249T>C
|
|
|
ENST00000675202.1:c.995T>C
|
ENSP00000502843.1:p.Met332Thr
|
|
ENST00000675331.1:c.995T>C
|
ENSP00000502031.1:p.Met332Thr
|
|
ENST00000675385.1:n.609T>C
|
|
|
ENST00000675390.1:c.995T>C
|
ENSP00000501969.1:p.Met332Thr
|
|
ENST00000675574.1:n.4050T>C
|
|
|
ENST00000675621.1:c.995T>C
|
ENSP00000502117.1:p.Met332Thr
|
|
ENST00000675764.1:c.*949T>C
|
ENSP00000502242.1:n.*949T>C
|
|
ENST00000676077.1:c.*313T>C
|
ENSP00000502507.1:n.*313T>C
|
|
ENST00000676098.1:c.995T>C
|
ENSP00000502735.1:p.Met332Thr
|
|
ENST00000676188.1:c.995T>C
|
ENSP00000502577.1:p.Met332Thr
|
|
ENST00000676353.1:c.800T>C
|
ENSP00000502737.1:p.Met267Thr
|
|
ENST00000397193.7:n.803T>C
|
|
|
ENST00000397195.9:c.995T>C
|
ENSP00000380378.4:p.Met332Thr
|
|
ENST00000571495.1:n.719T>C
|
|
|
ENST00000572915.6:n.676+2503T>C
|
|
|
ENST00000574468.1:c.396+2311T>C
|
ENSP00000460591.1:n.396+2311T>C
|
|
ENST00000574816.5:n.316T>C
|
|
|
NM_000430.3:c.995T>C
|
NP_000421.1:p.Met332Thr
|
|
XM_011523901.1:c.1049T>C
|
XP_011522203.1:p.Met350Thr
|
|
XM_011523902.1:c.1049T>C
|
XP_011522204.1:p.Met350Thr
|
|
XM_011523903.1:c.1049T>C
|
XP_011522205.1:p.Met350Thr
|
|
XM_011523901.2:c.1049T>C
|
XP_011522203.1:p.Met350Thr
|
|
XM_011523902.3:c.1049T>C
|
XP_011522204.1:p.Met350Thr
|
|
XM_011523903.2:c.1049T>C
|
XP_011522205.1:p.Met350Thr
|
|
XM_017024701.1:c.995T>C
|
XP_016880190.1:p.Met332Thr
|
|
XM_017024702.2:c.800T>C
|
XP_016880191.1:p.Met267Thr
|
|
NM_000430.4:c.995T>C
MANE Select
|
NP_000421.1:p.Met332Thr
|
|