ENST00000331373.10:c.*16A>C
MANE Select
|
ENSP00000331258.5:n.*16A>C
|
|
ENST00000614426.2:c.*865A>C
|
ENSP00000478821.2:n.*865A>C
|
|
ENST00000674646.1:c.787A>C
|
ENSP00000501703.1:n.787A>C
|
|
ENST00000674676.1:c.787A>C
|
ENSP00000502544.1:n.787A>C
|
|
ENST00000674782.1:c.*989A>C
|
ENSP00000501683.1:n.*989A>C
|
|
ENST00000674937.1:c.*16A>C
|
ENSP00000501823.1:n.*16A>C
|
|
ENST00000675322.1:c.787A>C
|
ENSP00000502235.1:n.787A>C
|
|
ENST00000675675.1:c.787A>C
|
ENSP00000501793.1:n.787A>C
|
|
ENST00000676178.1:c.*854A>C
|
ENSP00000502007.1:n.*854A>C
|
|
ENST00000676193.1:c.*16A>C
|
ENSP00000502774.1:n.*16A>C
|
|
ENST00000331373.9:c.*16A>C
|
ENSP00000331258.5:n.*16A>C
|
|
ENST00000614426.1:c.*16A>C
|
ENSP00000478821.1:n.*16A>C
|
|
NM_001277971.1:c.*16A>C
|
NP_001264900.1:n.*16A>C
|
|
NM_032237.4:c.*16A>C
|
NP_115613.1:n.*16A>C
|
|
XM_011544668.1:c.*16A>C
|
XP_011542970.1:n.*16A>C
|
|
XM_011544669.1:c.*16A>C
|
XP_011542971.1:n.*16A>C
|
|
NM_032237.5:c.*16A>C
MANE Select
|
NP_115613.1:n.*16A>C
|
|
NM_001277971.2:c.*16A>C
|
NP_001264900.1:n.*16A>C
|
|