ENST00000331373.10:c.576G>T
MANE Select
|
ENSP00000331258.5:p.Leu192=
|
|
ENST00000614426.2:c.*372G>T
|
ENSP00000478821.2:n.*372G>T
|
|
ENST00000674646.1:c.294G>T
|
ENSP00000501703.1:p.Leu98=
|
|
ENST00000674676.1:c.294G>T
|
ENSP00000502544.1:p.Leu98=
|
|
ENST00000674782.1:c.*496G>T
|
ENSP00000501683.1:n.*496G>T
|
|
ENST00000674937.1:c.534G>T
|
ENSP00000501823.1:p.Leu178=
|
|
ENST00000675322.1:c.294G>T
|
ENSP00000502235.1:p.Leu98=
|
|
ENST00000675675.1:c.294G>T
|
ENSP00000501793.1:p.Leu98=
|
|
ENST00000676178.1:c.*361G>T
|
ENSP00000502007.1:n.*361G>T
|
|
ENST00000676193.1:c.576G>T
|
ENSP00000502774.1:p.Leu192=
|
|
ENST00000331373.9:c.576G>T
|
ENSP00000331258.5:p.Leu192=
|
|
ENST00000614426.1:c.576G>T
|
ENSP00000478821.1:p.Leu192=
|
|
NM_001277971.1:c.576G>T
|
NP_001264900.1:p.Leu192=
|
|
NM_032237.4:c.576G>T
|
NP_115613.1:p.Leu192=
|
|
XM_011544668.1:c.576G>T
|
XP_011542970.1:p.Leu192=
|
|
XM_011544669.1:c.576G>T
|
XP_011542971.1:p.Leu192=
|
|
NM_032237.5:c.576G>T
MANE Select
|
NP_115613.1:p.Leu192=
|
|
NM_001277971.2:c.576G>T
|
NP_001264900.1:p.Leu192=
|
|