ENST00000696192.1:c.*832C>T
(F12)
|
ENSP00000512476.1:n.*832C>T
|
|
ENST00000696193.1:c.*1553C>T
(F12)
|
ENSP00000512477.1:n.*1553C>T
|
|
ENST00000696194.1:c.*756C>T
(F12)
|
ENSP00000512478.1:n.*756C>T
|
|
ENST00000696195.1:n.3969C>T
(F12)
|
|
|
ENST00000696200.1:n.1269C>T
(F12)
|
|
|
ENST00000696201.1:c.1166C>T
(F12)
|
ENSP00000512482.1:p.Ala389Val
|
|
ENST00000253496.4:c.1166C>T
(F12)
MANE Select
|
ENSP00000253496.3:p.Ala389Val
|
|
ENST00000253496.3:c.1166C>T
(F12)
|
ENSP00000253496.3:p.Ala389Val
|
|
ENST00000502598.5:c.-45+417G>A
(GRK6)
|
ENSP00000422873.1:n.-45+417G>A
|
|
ENST00000502854.5:n.425C>T
(F12)
|
|
|
ENST00000503736.1:n.538C>T
(F12)
|
|
|
ENST00000510358.5:n.530C>T
(F12)
|
|
|
NM_000505.3:c.1166C>T , LRG_145t1:c.1166C>T
(F12)
|
NP_000496.2:p.Ala389Val
|
|
XM_011534461.1:c.1166C>T
(F12)
|
XP_011532763.1:p.Ala389Val
|
|
XM_011534462.1:c.830C>T
(F12)
|
XP_011532764.1:p.Ala277Val
|
|
XM_011534462.2:c.830C>T
(F12)
|
XP_011532764.1:p.Ala277Val
|
|
XM_017009773.2:c.1416+6869G>A
(SLC34A1)
|
XP_016865262.1:n.1416+6869G>A
|
|
NM_000505.4:c.1166C>T
(F12)
MANE Select
|
NP_000496.2:p.Ala389Val
|
|