|
ENST00000383772.9:c.659T>C
|
ENSP00000373282.5:p.Leu220Pro
|
|
|
ENST00000437042.7:c.302T>C
|
ENSP00000398840.2:p.Leu101Pro
|
|
|
ENST00000458646.2:c.302T>C
|
ENSP00000391391.1:p.Leu101Pro
|
|
|
ENST00000462272.6:n.583T>C
|
|
|
|
ENST00000479097.6:c.*27T>C
|
ENSP00000508755.1:n.*27T>C
|
|
|
ENST00000480001.6:c.638T>C
|
ENSP00000510647.1:p.Leu213Pro
|
|
|
ENST00000685523.1:c.*474T>C
|
ENSP00000508765.1:n.*474T>C
|
|
|
ENST00000686715.1:c.659T>C
|
ENSP00000510539.1:p.Leu220Pro
|
|
|
ENST00000687083.1:c.638T>C
|
ENSP00000509681.1:p.Leu213Pro
|
|
|
ENST00000687353.1:c.659T>C
|
ENSP00000508588.1:p.Leu220Pro
|
|
|
ENST00000687676.1:c.659T>C
|
ENSP00000510313.1:p.Leu220Pro
|
|
|
ENST00000688892.1:c.659T>C
|
ENSP00000510650.1:p.Leu220Pro
|
|
|
ENST00000689700.1:c.332T>C
|
ENSP00000510200.1:p.Leu111Pro
|
|
|
ENST00000690398.1:c.*253T>C
|
ENSP00000510044.1:n.*253T>C
|
|
|
ENST00000691580.1:c.467T>C
|
|
|
|
ENST00000691912.1:c.638T>C
|
ENSP00000510520.1:p.Leu213Pro
|
|
|
ENST00000693261.1:c.302T>C
|
ENSP00000508421.1:p.Leu101Pro
|
|
|
ENST00000693580.1:c.303+10656T>C
|
ENSP00000510405.1:n.303+10656T>C
|
|
|
ENST00000330688.9:c.638T>C
MANE Select
|
ENSP00000332296.4:p.Leu213Pro
|
|
|
ENST00000330688.8:c.638T>C
|
ENSP00000332296.4:p.Leu213Pro
|
|
|
ENST00000383772.8:c.659T>C
|
ENSP00000373282.4:p.Leu220Pro
|
|
|
ENST00000437042.6:c.302T>C
|
ENSP00000398840.2:p.Leu101Pro
|
|
|
ENST00000458646.1:c.302T>C
|
ENSP00000391391.1:p.Leu101Pro
|
|
|
ENST00000462272.5:n.654T>C
|
|
|
|
ENST00000479097.5:n.493T>C
|
|
|
|
ENST00000480001.5:n.654T>C
|
|
|
|
NM_000965.4:c.638T>C
|
NP_000956.2:p.Leu213Pro
|
|
|
NM_001290216.1:c.659T>C
|
NP_001277145.1:p.Leu220Pro
|
|
|
NM_001290217.1:c.302T>C
|
NP_001277146.1:p.Leu101Pro
|
|
|
NM_001290266.1:c.491T>C
|
NP_001277195.1:p.Leu164Pro
|
|
|
NM_001290276.1:c.302T>C
|
NP_001277205.1:p.Leu101Pro
|
|
|
NM_001290277.1:c.638T>C
|
NP_001277206.1:p.Leu213Pro
|
|
|
NM_001290300.1:c.509T>C
|
NP_001277229.1:p.Leu170Pro
|
|
|
NM_016152.3:c.302T>C
|
NP_057236.1:p.Leu101Pro
|
|
|
NR_110892.1:n.946T>C
|
|
|
|
NR_110893.1:n.1107T>C
|
|
|
|
NM_001290216.2:c.659T>C
|
NP_001277145.1:p.Leu220Pro
|
|
|
NM_000965.5:c.638T>C
MANE Select
|
NP_000956.2:p.Leu213Pro
|
|
|
NM_001290216.3:c.659T>C
|
NP_001277145.1:p.Leu220Pro
|
|
|
NM_001290217.2:c.302T>C
|
NP_001277146.1:p.Leu101Pro
|
|
|
NM_001290266.2:c.491T>C
|
NP_001277195.1:p.Leu164Pro
|
|
|
NM_001290276.2:c.302T>C
|
NP_001277205.1:p.Leu101Pro
|
|
|
NM_001290300.2:c.509T>C
|
NP_001277229.1:p.Leu170Pro
|
|
|
NM_016152.4:c.302T>C
|
NP_057236.1:p.Leu101Pro
|
|
|
NR_110892.2:n.946T>C
|
|
|
|
NR_110893.2:n.1107T>C
|
|
|
