ENST00000697843.1:n.2396G>T
|
|
|
ENST00000373189.6:c.920G>T
MANE Select
|
ENSP00000362285.5:p.Ser307Ile
|
|
ENST00000479577.2:c.686G>T
|
ENSP00000493995.1:p.Ser229Ile
|
|
ENST00000642198.1:c.*492G>T
|
ENSP00000494827.1:n.*492G>T
|
|
ENST00000642772.1:c.*94+5857G>T
|
ENSP00000495041.1:n.*94+5857G>T
|
|
ENST00000643042.1:c.541G>T
|
ENSP00000496674.1:n.541G>T
|
|
ENST00000643619.1:c.*503G>T
|
ENSP00000494378.1:n.*503G>T
|
|
ENST00000643752.1:c.*246G>T
|
ENSP00000495000.1:n.*246G>T
|
|
ENST00000644088.1:c.*241G>T
|
ENSP00000494066.1:n.*241G>T
|
|
ENST00000644591.1:c.*246G>T
|
ENSP00000496664.1:n.*246G>T
|
|
ENST00000644895.1:c.*99+5857G>T
|
ENSP00000493872.1:n.*99+5857G>T
|
|
ENST00000645345.1:c.*492G>T
|
ENSP00000495859.1:n.*492G>T
|
|
ENST00000647524.1:c.*503G>T
|
ENSP00000495077.1:n.*503G>T
|
|
ENST00000373189.5:c.920G>T
|
ENSP00000362285.5:p.Ser307Ile
|
|
ENST00000469204.1:n.417G>T
|
|
|
NM_001174098.1:c.*149G>T
|
NP_001167569.1:n.*149G>T
|
|
NM_018344.5:c.920G>T
|
NP_060814.4:p.Ser307Ile
|
|
NR_033413.1:n.894G>T
|
|
|
NR_033414.1:n.667G>T
|
|
|
XM_006717910.2:c.686G>T
|
XP_006717973.1:p.Ser229Ile
|
|
NM_001363518.1:c.686G>T
|
NP_001350447.1:p.Ser229Ile
|
|
XM_017016377.2:c.482G>T
|
XP_016871866.1:p.Ser161Ile
|
|
XM_017016378.2:c.302G>T
|
XP_016871867.1:p.Ser101Ile
|
|
NM_018344.6:c.920G>T
MANE Select
|
NP_060814.4:p.Ser307Ile
|
|
NM_001174098.2:c.*149G>T
|
NP_001167569.1:n.*149G>T
|
|
NM_001363518.2:c.686G>T
|
NP_001350447.1:p.Ser229Ile
|
|
NR_033413.2:n.888G>T
|
|
|
NR_033414.2:n.661G>T
|
|
|