ENST00000696192.1:c.*455C>T
(F12)
|
ENSP00000512476.1:n.*455C>T
|
|
ENST00000696193.1:c.*1159C>T
(F12)
|
ENSP00000512477.1:n.*1159C>T
|
|
ENST00000696194.1:c.*379C>T
(F12)
|
ENSP00000512478.1:n.*379C>T
|
|
ENST00000696195.1:n.3592C>T
(F12)
|
|
|
ENST00000696200.1:n.892C>T
(F12)
|
|
|
ENST00000696201.1:c.789C>T
(F12)
|
ENSP00000512482.1:p.His263=
|
|
ENST00000253496.4:c.789C>T
(F12)
MANE Select
|
ENSP00000253496.3:p.His263=
|
|
ENST00000253496.3:c.789C>T
(F12)
|
ENSP00000253496.3:p.His263=
|
|
ENST00000502598.5:c.-45+984G>A
(GRK6)
|
ENSP00000422873.1:n.-45+984G>A
|
|
ENST00000503736.1:n.173-97C>T
(F12)
|
|
|
ENST00000506296.5:c.-92G>A
(GRK6)
|
ENSP00000421055.1:n.-92G>A
|
|
NM_000505.3:c.789C>T , LRG_145t1:c.789C>T
(F12)
|
NP_000496.2:p.His263=
|
|
XM_011534461.1:c.789C>T
(F12)
|
XP_011532763.1:p.His263=
|
|
XM_011534462.1:c.453C>T
(F12)
|
XP_011532764.1:p.His151=
|
|
XM_011534462.2:c.453C>T
(F12)
|
XP_011532764.1:p.His151=
|
|
XM_017009773.2:c.1417-7254G>A
(SLC34A1)
|
XP_016865262.1:n.1417-7254G>A
|
|
NM_000505.4:c.789C>T
(F12)
MANE Select
|
NP_000496.2:p.His263=
|
|