ENST00000696192.1:c.*431G>T
(F12)
|
ENSP00000512476.1:n.*431G>T
|
|
ENST00000696193.1:c.*1135G>T
(F12)
|
ENSP00000512477.1:n.*1135G>T
|
|
ENST00000696194.1:c.*355G>T
(F12)
|
ENSP00000512478.1:n.*355G>T
|
|
ENST00000696195.1:n.3568G>T
(F12)
|
|
|
ENST00000696200.1:n.868G>T
(F12)
|
|
|
ENST00000696201.1:c.765G>T
(F12)
|
ENSP00000512482.1:p.Ala255=
|
|
ENST00000253496.4:c.765G>T
(F12)
MANE Select
|
ENSP00000253496.3:p.Ala255=
|
|
ENST00000253496.3:c.765G>T
(F12)
|
ENSP00000253496.3:p.Ala255=
|
|
ENST00000502598.5:c.-45+1008C>A
(GRK6)
|
ENSP00000422873.1:n.-45+1008C>A
|
|
ENST00000503736.1:n.173-121G>T
(F12)
|
|
|
ENST00000506296.5:c.-68C>A
(GRK6)
|
ENSP00000421055.1:n.-68C>A
|
|
NM_000505.3:c.765G>T , LRG_145t1:c.765G>T
(F12)
|
NP_000496.2:p.Ala255=
|
|
XM_011534461.1:c.765G>T
(F12)
|
XP_011532763.1:p.Ala255=
|
|
XM_011534462.1:c.429G>T
(F12)
|
XP_011532764.1:p.Ala143=
|
|
XM_011534462.2:c.429G>T
(F12)
|
XP_011532764.1:p.Ala143=
|
|
XM_017009773.2:c.1417-7230C>A
(SLC34A1)
|
XP_016865262.1:n.1417-7230C>A
|
|
NM_000505.4:c.765G>T
(F12)
MANE Select
|
NP_000496.2:p.Ala255=
|
|