ENST00000331373.10:c.999G>A
MANE Select
|
ENSP00000331258.5:p.Lys333=
|
|
ENST00000614426.2:c.*795G>A
|
ENSP00000478821.2:n.*795G>A
|
|
ENST00000674646.1:c.717G>A
|
ENSP00000501703.1:p.Lys239=
|
|
ENST00000674676.1:c.717G>A
|
ENSP00000502544.1:p.Lys239=
|
|
ENST00000674782.1:c.*919G>A
|
ENSP00000501683.1:n.*919G>A
|
|
ENST00000674937.1:c.957G>A
|
ENSP00000501823.1:p.Lys319=
|
|
ENST00000675322.1:c.717G>A
|
ENSP00000502235.1:p.Lys239=
|
|
ENST00000675675.1:c.717G>A
|
ENSP00000501793.1:p.Lys239=
|
|
ENST00000676178.1:c.*784G>A
|
ENSP00000502007.1:n.*784G>A
|
|
ENST00000676193.1:c.999G>A
|
ENSP00000502774.1:p.Lys333=
|
|
ENST00000331373.9:c.999G>A
|
ENSP00000331258.5:p.Lys333=
|
|
ENST00000614426.1:c.999G>A
|
ENSP00000478821.1:p.Lys333=
|
|
NM_001277971.1:c.999G>A
|
NP_001264900.1:p.Lys333=
|
|
NM_032237.4:c.999G>A
|
NP_115613.1:p.Lys333=
|
|
XM_011544668.1:c.999G>A
|
XP_011542970.1:p.Lys333=
|
|
XM_011544669.1:c.999G>A
|
XP_011542971.1:p.Lys333=
|
|
NM_032237.5:c.999G>A
MANE Select
|
NP_115613.1:p.Lys333=
|
|
NM_001277971.2:c.999G>A
|
NP_001264900.1:p.Lys333=
|
|