ENST00000696192.1:c.*570G>A
(F12)
|
ENSP00000512476.1:n.*570G>A
|
|
ENST00000696193.1:c.*1274G>A
(F12)
|
ENSP00000512477.1:n.*1274G>A
|
|
ENST00000696194.1:c.*494G>A
(F12)
|
ENSP00000512478.1:n.*494G>A
|
|
ENST00000696195.1:n.3707G>A
(F12)
|
|
|
ENST00000696200.1:n.1007G>A
(F12)
|
|
|
ENST00000696201.1:c.904G>A
(F12)
|
ENSP00000512482.1:p.Ala302Thr
|
|
ENST00000253496.4:c.904G>A
(F12)
MANE Select
|
ENSP00000253496.3:p.Ala302Thr
|
|
ENST00000253496.3:c.904G>A
(F12)
|
ENSP00000253496.3:p.Ala302Thr
|
|
ENST00000502598.5:c.-45+784C>T
(GRK6)
|
ENSP00000422873.1:n.-45+784C>T
|
|
ENST00000502854.5:n.163G>A
(F12)
|
|
|
ENST00000503736.1:n.276G>A
(F12)
|
|
|
ENST00000510358.5:n.163G>A
(F12)
|
|
|
NM_000505.3:c.904G>A , LRG_145t1:c.904G>A
(F12)
|
NP_000496.2:p.Ala302Thr
|
|
XM_011534461.1:c.904G>A
(F12)
|
XP_011532763.1:p.Ala302Thr
|
|
XM_011534462.1:c.568G>A
(F12)
|
XP_011532764.1:p.Ala190Thr
|
|
XM_011534462.2:c.568G>A
(F12)
|
XP_011532764.1:p.Ala190Thr
|
|
XM_017009773.2:c.1416+7236C>T
(SLC34A1)
|
XP_016865262.1:n.1416+7236C>T
|
|
NM_000505.4:c.904G>A
(F12)
MANE Select
|
NP_000496.2:p.Ala302Thr
|
|