|
ENST00000355906.10:c.498C>T
(HP)
MANE Select
|
ENSP00000348170.5:p.His166=
|
|
|
ENST00000228226.12:c.123C>T
(HP)
|
ENSP00000228226.9:p.His41=
|
|
|
ENST00000355906.9:c.498C>T
(HP)
|
ENSP00000348170.5:p.His166=
|
|
|
ENST00000357763.8:c.606C>T
(HP)
|
ENSP00000350406.5:p.His202=
|
|
|
ENST00000398131.6:c.321C>T
(HP)
|
ENSP00000381199.2:p.His107=
|
|
|
ENST00000562153.5:c.285-15810G>A
(TXNL4B)
|
ENSP00000454635.1:n.285-15810G>A
|
|
|
ENST00000562526.5:c.266-496C>T
(HP)
|
ENSP00000454413.1:n.266-496C>T
|
|
|
ENST00000564499.5:c.266-65C>T
(HP)
|
ENSP00000456503.1:n.266-65C>T
|
|
|
ENST00000565574.5:c.321C>T
(HP)
|
ENSP00000454966.1:p.His107=
|
|
|
ENST00000566821.1:n.2137C>T
(HP)
|
|
|
|
ENST00000567185.7:c.490C>T
(HP)
|
|
|
|
ENST00000567612.2:c.438-65C>T
(HP)
|
|
|
|
ENST00000570083.5:c.321C>T
(HP)
|
ENSP00000457629.1:p.His107=
|
|
|
ENST00000613898.1:c.123C>T
(HP)
|
ENSP00000478279.1:p.His41=
|
|
|
NM_001126102.1:c.321C>T
(HP)
|
NP_001119574.1:p.His107=
|
|
|
NM_005143.3:c.498C>T
(HP)
|
NP_005134.1:p.His166=
|
|
|
XM_005255922.3:c.321C>T
(HP)
|
XP_005255979.2:p.His107=
|
|
|
NM_001126102.2:c.321C>T
(HP)
|
NP_001119574.1:p.His107=
|
|
|
NM_001318138.1:c.321C>T
(HP)
|
NP_001305067.1:p.His107=
|
|
|
NM_005143.4:c.498C>T
(HP)
|
NP_005134.1:p.His166=
|
|
|
XM_017023377.2:c.285-15810G>A
(TXNL4B)
|
XP_016878866.1:n.285-15810G>A
|
|
|
NM_001318138.2:c.321C>T
(HP)
|
NP_001305067.1:p.His107=
|
|
|
NM_005143.5:c.498C>T
(HP)
MANE Select
|
NP_005134.1:p.His166=
|
|
|
NM_001126102.3:c.321C>T
(HP)
|
NP_001119574.1:p.His107=
|
|
