ENST00000403733.8:c.3191G>T
MANE Select
|
ENSP00000384222.3:p.Arg1064Leu
|
|
ENST00000403733.7:c.3191G>T
|
ENSP00000384222.3:p.Arg1064Leu
|
|
ENST00000427431.5:c.*2583G>T
|
ENSP00000393342.1:n.*2583G>T
|
|
ENST00000438543.5:c.*987G>T
|
ENSP00000413521.1:n.*987G>T
|
|
ENST00000448232.6:c.3263G>T
|
ENSP00000398577.2:p.Arg1088Leu
|
|
ENST00000504005.5:c.2237G>T
|
ENSP00000427569.1:p.Arg746Leu
|
|
ENST00000508747.1:c.575G>T
|
ENSP00000420835.1:p.Arg192Leu
|
|
ENST00000513834.5:c.3044G>T
|
ENSP00000425054.1:p.Arg1015Leu
|
|
NM_024949.5:c.3191G>T
|
NP_079225.5:p.Arg1064Leu
|
|
XM_011532269.1:c.3263G>T
|
XP_011530571.1:p.Arg1088Leu
|
|
XM_011532269.3:c.3263G>T
|
XP_011530571.1:p.Arg1088Leu
|
|
XM_024454225.1:c.2969G>T
|
XP_024309993.1:p.Arg990Leu
|
|
NM_024949.6:c.3191G>T
MANE Select
|
NP_079225.5:p.Arg1064Leu
|
|