ENST00000700472.1:c.*569G>T
|
ENSP00000515005.1:n.*569G>T
|
|
ENST00000264033.6:c.1117G>T
MANE Select
|
ENSP00000264033.3:p.Glu373Ter
|
|
ENST00000637974.1:c.1111G>T
|
ENSP00000490763.1:p.Glu371Ter
|
|
ENST00000264033.5:c.1117G>T
|
ENSP00000264033.3:p.Glu373Ter
|
|
ENST00000634586.1:c.1117G>T
|
ENSP00000489218.1:p.Glu373Ter
|
|
ENST00000634840.1:c.1117G>T
|
ENSP00000489324.1:p.Glu373Ter
|
|
NM_005188.3:c.1117G>T , LRG_608t1:c.1117G>T
|
NP_005179.2:p.Glu373Ter
|
|
XM_011543057.1:c.1117G>T
|
XP_011541359.1:p.Glu373Ter
|
|
NM_005188.4:c.1117G>T
MANE Select
|
NP_005179.2:p.Glu373Ter
|
|