|
ENST00000355906.10:c.516C>T
(HP)
MANE Select
|
ENSP00000348170.5:p.Ser172=
|
|
|
ENST00000228226.12:c.141C>T
(HP)
|
ENSP00000228226.9:p.Ser47=
|
|
|
ENST00000355906.9:c.516C>T
(HP)
|
ENSP00000348170.5:p.Ser172=
|
|
|
ENST00000357763.8:c.624C>T
(HP)
|
ENSP00000350406.5:p.Ser208=
|
|
|
ENST00000398131.6:c.339C>T
(HP)
|
ENSP00000381199.2:p.Ser113=
|
|
|
ENST00000562153.5:c.285-15828G>A
(TXNL4B)
|
ENSP00000454635.1:n.285-15828G>A
|
|
|
ENST00000562526.5:c.266-478C>T
(HP)
|
ENSP00000454413.1:n.266-478C>T
|
|
|
ENST00000564499.5:c.266-47C>T
(HP)
|
ENSP00000456503.1:n.266-47C>T
|
|
|
ENST00000565574.5:c.339C>T
(HP)
|
ENSP00000454966.1:p.Ser113=
|
|
|
ENST00000566821.1:n.2155C>T
(HP)
|
|
|
|
ENST00000567185.7:c.508C>T
(HP)
|
|
|
|
ENST00000567612.2:c.438-47C>T
(HP)
|
|
|
|
ENST00000570083.5:c.339C>T
(HP)
|
ENSP00000457629.1:p.Ser113=
|
|
|
ENST00000613898.1:c.141C>T
(HP)
|
ENSP00000478279.1:p.Ser47=
|
|
|
NM_001126102.1:c.339C>T
(HP)
|
NP_001119574.1:p.Ser113=
|
|
|
NM_005143.3:c.516C>T
(HP)
|
NP_005134.1:p.Ser172=
|
|
|
XM_005255922.3:c.339C>T
(HP)
|
XP_005255979.2:p.Ser113=
|
|
|
NM_001126102.2:c.339C>T
(HP)
|
NP_001119574.1:p.Ser113=
|
|
|
NM_001318138.1:c.339C>T
(HP)
|
NP_001305067.1:p.Ser113=
|
|
|
NM_005143.4:c.516C>T
(HP)
|
NP_005134.1:p.Ser172=
|
|
|
XM_017023377.2:c.285-15828G>A
(TXNL4B)
|
XP_016878866.1:n.285-15828G>A
|
|
|
NM_001318138.2:c.339C>T
(HP)
|
NP_001305067.1:p.Ser113=
|
|
|
NM_005143.5:c.516C>T
(HP)
MANE Select
|
NP_005134.1:p.Ser172=
|
|
|
NM_001126102.3:c.339C>T
(HP)
|
NP_001119574.1:p.Ser113=
|
|
